Lymphatic filariasis: new insights and prospects for control Thomas B. Nutman
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1 Lymphatic filariasis: new insights and prospects for control Thomas B Nutman Although lymphatic filariasis remains among the major causes of disability among the tropical infectious diseases, dramatic advances have been made in the approach to its diagnosis, epidemiology and treatment, in our understanding of the molecular composition of the parasites that cause these infections, and in the factors underlying the pathology seen Superimposing the tools of modern epidemiology, immunology, and molecular biology on field-based clinical trials has allowed the emergence of the concept of elimination of lymphatic filariasis Much of the important new research emphasizes parasite development in the context of the host response, the importance of both the adult worm and other factors in the pathogenesis of lymphatic filarial disease, the role the Wolbachia endosymbiont holds as both a target for drug treatment and in inducing post-treatment reactions, and the various principles underlying the implementation of control programs Curr Opin Infect Dis 14:539±546 # 2001 Lippincott Williams & Wilkins Helminth Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA Correspondence to Thomas B Nutman MD, Head, Helminth Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD , USA Tel: ; fax: ; tnutman@niaidnihgov Current Opinion in Infectious Diseases 2001, 14:539±546 Abbreviation IFNg interferon-gamma # 2001 Lippincott Williams & Wilkins Introduction Among the approximately 129 million patients infected with one of three lymph-dwelling lariae ± Wuchereria bancrofti, Brugia malayi, or B timori ± W bancrofti is responsible for the overwhelming majority (*115 million) [1 ] Although there are many differing clinical manifestations of longstanding infection with the lymphatic lariases (hydrocele, recurrent adenolymphangitis, lymphedema, elephantiasis or tropical pulmonary eosinophilia ± see [2 ] for a comprehensive review), the most intriguing (from an immunological perspective) is a subclinical condition associated with high levels of circulating micro lariae (or parasite antigen) Indeed, in areas where W bancrofti or B malayi are endemic, the overwhelming majority of infected individuals have few overt clinical manifestations of their larial infection despite the presence of circulating micro lariae (or parasite antigen) in the peripheral blood Although they may be clinically asymptomatic, virtually all persons with patent W bancrofti or B malayi infection have some degree of subclinical disease that includes microscopic hematuria or proteinuria [3], dilated (and tortuous) lymphatics when imaged [4,5,6 ] and, in men with W bancrofti infection, scrotal lymphangiectasia [7 ] This subclinical majority notwithstanding, current estimates suggest that lymphatic lariasis, among the reported tropical diseases, is responsible for the third most global burden of disease (behind malaria and tuberculosis) with a burden estimated at disability-adjusted life years lost [8] The parasite W bancrofti and the two Brugia species are transmitted by mosquitoes Each goes through a complex life cycle that includes an infective larval stage (L3) carried by the insects and an adult worm stage that can be found either in the lymph nodes or adjacent lymphatics The offspring of the adults, the micro lariae (220±280 mm long and 5±7 mm wide), circulate in the blood These micro lariae then can be ingested by a biting mosquito where they develop in the arthropod over a 1±2 week period into infective larvae, which are in turn capable of re-initiating the life cycle Parasite development Many aspects of the developmental biology of larial parasites await elucidation This lack of insight has stemmed, in part, from the lack of consistent in-vitro methods for culturing the early life cycle stages of the parasite [9 ], particularly using de ned conditions A serum-free system has been developed that supports the 539
2 540 Tropical and travel-associated diseases development of the infective stage larvae (L3) into viable fourth-stage larvae [10], providing the capability, at least, to examine the minimum requirements for early parasite development in the mammalian host Parasite genetics and molecular biology The larial nuclear genome (based primarily on work done with B malayi) is estimated to be around 100 million base pairs, about the same size as that of the free living nematode Caenorhabditis elegans The genome is AT rich (71%) and is divided among ve pairs of chromosomes (four pairs of autosomes and one pair of sex chromosomes) Within the parasite two other genomes are found, the rst being a mitochondrial genome and the second being the genome of the bacterial endosymbiont (see below) The Filarial Genome Project, established in 1994, focused on gene discovery using an expressed sequence tag approach Thus far, more than expressed sequence tags have been completed, and more than 7000 genes have been identi ed [11 ] There is a new initiative to sequence the entire genome as this approach is now more feasible given the advances in sequencing technologies The population biology of any of the lariae is poorly understood, and approaches relying on repeated sequences (used primarily for diagnostics) of DNA have failed to consistently identify signi cant diversity among related isolates [12,13] Recently, microsatellite loci from B malayi have been able to reliably distinguish among isolates from differing geographic locations [14 ] This methodologic `proof of principle' should help to address important population genetic questions in larial biology such as drug susceptibility, emergence of new isolates, genetic bases of periodicity, among others Additional attention has also been focused on individual molecules that may be targets for chemotherapy [15,16] and vaccine development [17,18,19 ]; moreover, there has been the molecular characterization of parasite molecules that may serve to modulate host immune functions such as T cell cytokine production or antigen presentation [20,21], induction of apoptosis [22] or those parasite transcription factors that may be regulated by host growth factors [23] Endosymbiont With the reemergence of interest in the intracellular Wolbachia endosymbiont of larial parasites [24,25] and the recent demonstration of their potential as targets for macro laricidal chemotherapy [26,27,28±32], there has been renewed attention paid to the biological makeup of the larial Wolbachiae [11,28,33,34,35] Indeed, there is not only a Wolbachia Genome Consortium in place to sequence the entire B malayi endosymbiont [11 ], but also, by using comparisons of the wsp, 16S rrna, and ftsz gene sequences, the phylogenetic relationships among various larial Wolbachiae and those of arthropods have been made [28,33,35] Moreover, there remains the possibility of transferring the endosymbionts from lariae to insect cell lines, already being utilized for maintaining insect endosymbionts, a process that will provide both material and methods to enable the study of the molecular organization of this critical intracellular bacterium [11 ] Clinical disease and its socioeconomic burdens Although many of the manifestations of lymphatic lariasis have been known for centuries, some much needed attention has recently been paid to several important clinical aspects These include an examination of the sexual dysfunction and reproductive health associated with genital disease in lymphatic lariasis [36,37,38] These studies have demonstrated quite clearly that the degree of sexual dysfunction, particularly among men with hydroceles and lymph scrotum [36,37], is great and relatively unexplored Moreover, qualitatively collected data on school age children in a larial endemic region of India suggested that hydoceles and adenolymphangitis played a major role in poor performance in school, absenteeism and dropout [39] As part of an ongoing effort to assess the economic burden of lymphatic lariasis, in India, for example, lymphatic lariasis has been estimated to be responsible for the loss of about 063% of the per capita gross national product [40 ] The economic impact was equally important in Ghana where it was found that in some communities more than 20% of all elective surgery was for hydrocele operations [41,42] Much of these and other data have been codi ed and reviewed by Haddix et al [43 ] Pathogenesis Recent evidence from detailed clinical, surgical and imaging (ultrasound or lymphoscintigraphy) observations and from immunohistologic analysis of tissue from lymphedematous limbs of affected patients has suggested that compromised lymphatic function and lymphangiectasia play a signi cant role in mediating some of the pathology associated with lymphatic larial infections [7,44] This type of pathology appears to be related to the presence of viable adult worms in the lymphatics or lymph nodes [44] Moreover, bacteriologic studies of tissue from lymphedematous limbs of affected patients [45] has implicated bacterial or fungal superinfections of limbs superimposed on already compromised lymphatic function as playing a signi cant role in triggering some episodes of adenolymphangitis which in turn may exacerbate the chronic obstructive changes in the lymphatics of affected patients These studies have
3 Lymphatic filariasis Nutman 541 shown that the acute process usually starts in the skin and then spreads along the lymphatics to the lymph nodes Based on these observations, some have proposed that the syndrome be renamed dermatolymphangioadenitis [46 ] Although the importance of any one among the many factors involved in the pathogenesis of lymphedema, hydroceles, and elephantiasis remains still a matter of debate, the relative paucity of pathology among those with `active' or patent infection ± the presence of micro lariae and adult worms (as assessed by circulating antigen assays, polymerase chain reaction of blood, or ultrasonography) ± and its association with the inability of patient cells to proliferate or produce interferongamma (IFNg) in response to parasite antigen has been consistently found [47] A useful paradigm with which to understand the changes that the immune responses undergo over time is to divide the larial infection into `acute' (or early) and chronic phases [48,49] The `early' or prepatent infections appear to be associated with establishment of parasite-speci c lymphocyte proliferation, cytokine production with a mixed (interleukin-2, IFNg, interleukin-4, interleukin-5) phenotype, marked eosinophilia, and elevated levels of parasite-speci c IgE These ndings have been bolstered by the studies in permissive animal models (eg jirds, cats, dogs, monkeys and chimpanzees) in which most of these features have been seen early in infection With the onset of patency (development of adult worms and appearance of micro- lariae in the blood), certain immune responses are profoundly altered [48,49] Most notably, there is a diminution of parasite-speci c lymphocyte proliferation, interleukin-2 and IFNg production and an increase in anti larial IgG4 and the production of the regulatory cytokines interleukin-10 and perhaps transforming growth factor-b The development of this downregulated immune response is determined not only by the duration of infection but also by parasite burden (number of adult worms and micro lariae), both of which can be a function of the intensity of transmission [50 ] In areas of intense transmission, infections are acquired at younger ages and higher parasite burdens likely occur Immunology The most recent immunological studies on lymphatic dwelling lariae fall into two discrete groups First are the studies in animal models (particularly rodents) which have been increasingly used to examine the fundamental nature of the immune response to infection, particularly as it relates to tolerance induction [51,52,53,54±57], innate immunity and resistance to infection [58,59±63] Studies in humans have focused recently on the nature of protective immunity to lymphatic lariasis [49,64,65,66 ] and the evolution of the immune response underlying this protection [67 ] The immunological basis for protective immunity in humans has been notoriously dif cult to de ne in part because diagnostic tools were not suf ciently sensitive to determine that an individual was truly free of infection and in part because longitudinally collected information on exposure and infection status was generally unavailable for at risk populations With these as caveats, protective immunity to the micro lariae of W bancrofti appeared to be related directly to levels of antibody to the micro larial sheath [68] In two separate studies examining the humoral responses in so-called `endemic normal' individuals ± those with a clear history of exposure but lacking clinical disease and circulating antigenemia ± resistance to infection was associated with both anti-carbohydrate antibodies of the IgG2 and IgG3 isotypes [65] or with antibodies directed against L3 surface antigens [64] Using assessments of both cellular and antibody responses in a cohort of subjects studied longitudinally over a 17-year period in the Cook Islands, endemic normal individuals appeared to maintain their ability to respond to parasite antigen with cytokine, proliferative and antibody responses to a much greater degree than did patently infected individuals [67 ] Modulation of the immune response in larial infections has been examined in animal models in the context of (1) CD4+ T cell subset differentiation (Th1 versus Th2) [53,55±57], or (2) antigen presenting cell function [51,52,53,54] Clearly associated with the modulation of the immune response is diminished expression of the important costimulatory molecule CD80 [51 ] on antigen presenting cells, antigen presenting cell nitric oxide production [52,69] and the recruitment and presence of `alternatively activated' macrophages that inhibit parasite-speci c lymphocyte proliferation [53,54] Using a murine model in which micro lariae were used to drive the immune response, even in the presence of induced IFNg, the Th2 response predominated [56] Taken together, these and other [55,57] studies suggest several basic mechanisms by which the immune response to lymphaticdwelling lariae become downregulated In murine studies examining both innate and adaptive immune responses as mediators of protective immunity in lymphatic lariasis, attention has been focused on the role of the interleukin-4, interleukin-5 and IFNg in mediating resistance to infection While no consensus has emerged, both interleukin-4 [60±62] and interleukin- 5 [63] have been shown to play a major role In addition, the nding that B1 B lymphocytes, cells that appear to be induced in response to phosphorylcholine containing antigens from the larial parasites, can mediate protection provides a link between the adaptive and innate immune mechanisms [58,59]
4 542 Tropical and travel-associated diseases Diagnosis Although the detection of the micro lariae in the blood has been the mainstay of the diagnosis of lymphatic lariasis, the identi cation of the motile adult worms within the lymphatics (termed the ` laria dance sign') using high-frequency ultrasound in conjunction with Doppler has been found quite useful for diagnosis of bancroftian lariasis Although the transfer of ultrasound diagnosis from W bancrofti to B malayi infection was assumed likely, to date ultrasonography has failed to detect the adult B malayi adults [70 ] For W bancrofti infection, at least, both of these methods have been largely supplanted by detection of circulating larial antigen There are currently two commercially available tests, one in an enzyme-linked immunosorbent assay format [71] and the other a rapid-format immunochromatographic card test; each of these assays have sensitivities that range from 96 to 100% and speci cities that approach 100% [72] Because there are currently no tests for circulating antigens in brugian lariasis, there have been attempts to improve the diagnosis of brugian lariasis To this end, recombinantly-produced antigens with speci city for B malayi have been identi ed and shown, in preliminary experiments, to improve the diagnostic sensitivities for these infections [73,74 ] Polymerase chain reaction based assays for DNA of W bancrofti and B malayi in blood have also been developed, with the method being of equivalent or greater sensitivity than standard parasitologic methods The utility of these molecular diagnostics, however, has not been well assessed using blood obtained when micro lariae are not present (eg day blood of nocturnally periodic lariae) In a number of recent studies, methodologies for detection of DNA free of intact parasites have been developed for B malayi infections [75,76,77 ], although such techniques have been less successful in bancroftian lariasis [78] Occasionally, diagnostic aspiration for cytologic examination or as a consequence of excisional biopsy results in the identi cation of micro lariae in the specimens [79±83] Treatment In support largely of efforts to assess the impact of treatment on transmission with an eye toward control and possible elimination of lymphatic lariasis as a public health problem, a number of studies using single dose treatment with diethylcarbamazine, albendazole, or ivermectin alone or in various combinations have been performed in multiple geographic settings [42,84±88] Based on the cumulative data from 17 studies conducted around the world with a cumulative total of more than individuals (with primarily W bancrofti infection), a review of the safety and ef cacy of the regimens to be used in the programs to eliminate lymphatic lariasis (albendazole + ivermectin or albendazole + diethylcarbamazine) suggests that the addition of albendazole to either diethylcarbamazine or ivermectin is no less safe than therapy with a single medication [89 ] and may provide additional anti larial ef cacy along with salutary effects on intestinal helminth infections [90,91 ] The macro laricidal effects of diethylcarbamazine or albendazole alone or in combination therapy ± assessed directly by ultrasound or indirectly by antigen detection assays ± have demonstrated a consistent but partial effect [44,89,92,93 ] Regimens of higher dosage, longer duration or newer combinations have been suggested, as has the addition of antibiotics to standard single dose therapy (as has been used recently for onchocerciasis [27 ]) New approaches to anti larial chemotherapy, which include targeting the endosymbiont of the lymphatic larial parasites with antibiotics, particularly the tetracyclines [29,32,94,95], appear to be the most promising way forward in macro laricidal therapy of the lymphdwelling lariae Although clinical studies in lymphatic lariasis have not been completed, data from Onchocerca volvulus (in humans) and larial infections in animal models suggest that this approach should be feasible [27,29±32] Further, it is possible that the release of the intracellular endosymbionts and their lipopolysaccharide is responsible for the early in ammatory reactions seen following treatment of lymphatic lariasis [26,96] Agents such as UMF-078 [97] and an extract from a medicinal plant [98] have been shown to be active against the adult worms of B pahangi; in other drug screens, however, neither phosphoramidate inhibitors of b-tubulin [99] nor a set of anticancer agents [100] have been shown to possess activity against the lymph dwelling lariae Control The development of a global program to eliminate lariasis came following a resolution by the World Health Assembly in 1997 [26,90,91,101,102] The principal goals of the program are to interrupt transmission of infection and alleviate and prevent the disability caused by the disease [91 ] Primarily using community wide distribution [103] of yearly single dose combination chemotherapy ± diethylcarbamazine + albendazole or ivermectin + albendazole (made possible by a donation of albendazole by SmithKline Beecham/GlaxoSmith- Kline (Greenford, Middlesex, UK) with an additional commitment of Merck & Company (Whitehouse Station, New Jersey, USA) to expand the donation of ivermectin to African countries in which onchocerciasis and lymphatic lariasis are co-endemic) ± for transmission
5 Lymphatic filariasis Nutman 543 interruption [103] and strategies focusing on hygiene and decreasing secondary bacterial and fungal infections for morbidity control, the Global Lymphatic Filariasis Programme was launched in the year 2000 [104±106] As part of this control program, detailed distribution maps of prevalence of lymphatic lariasis were deemed a priority Using a variety of approaches including Geographic Information Systems [107], climate generated risk pro les [108 ], detection of circulating antigen [109,110], rapid assessments using questionnaires involving hydrocele or lymphedema presence [111], rates of hydrocelectomy as a proxy for hydrocele prevalence or the more traditional methods of micro larial surveys and clinical examinations [112±115], better mapping of lymphatic lariasis distribution is underway Other tools developed for the control effort include mathematical models for describing transmission dynamics [116,117] and its control; social and economic projections for quantifying the impact of lymphatic lariasis on society and the cost and bene ts of implementing control [43,118,119]; training in clinical management with an emphasis on morbidity control [44,120,121]; and consideration of methods to certify elimination [122] An ancillary bene t from these control programs will be the treatment of hookworm and other intestinal parasite infections by albendazole and ivermectin [89,123,124], and the treatment of ectoparasites (lice/ scabies) by ivermectin [125 ] and the hope of improved nutrition and cognitive function [91,126] Conclusion The elimination of lymphatic lariasis as a public health problem as a concept has emerged on the shoulders of extremely sound basic and clinical research The programs based on its implementation will require redoubled research efforts to provide, among others, new targets for intervention, improved methods for assessing infection status at both the individual and community level, testing for emergence of drug resistance, and operational answers to the problem of drug distribution, cost and socioeconomic impact of lymphatic lariasis References and recommended reading Papers of particular interest, published within the annual period of review, have been highlighted as: of special interest of outstanding interest 1 Michael E The population dynamics and epidemiology of lymphatic filariasis In: Lymphatic filariasis Tropical medicine: science and practice, Vol 1 Nutman TB (editor) London: Imperial College Press; 2000 pp 41±82 A comprehensive examination of the population dynamics based on observations and mathematical models 2 Kumaraswami V The clinical manifestations of lymphatic filariasis In: Lymphatic filariasis Tropical medicine: science and practice, Vol 1 Nutman TB (editor) London: Imperial College Press; 2000 pp 103±126 A detailed look at the clinical manifestations seen with infection with W bancrofti and B malayi 3 Dreyer G, Ottesen EA, Galdino E, et al Renal abnormalities in microfilaremic patients with bancroftian filariasis Am J Trop Med Hyg 1992; 46:745±751 4 Freedman DO, de Almeida Filho PJ, Besh S, et al Lymphoscintigraphic analysis of lymphatic abnormalities in symptomatic and asymptomatic human filariasis J Infect Dis 1994; 170:927±933 5 Freedman DO, Bui T, De Almeida Filho PJ, et al Lymphoscintigraphic assessment of the effect of diethylcarbamazine treatment on lymphatic damage in human bancroftian filariasis Am J Trop Med Hyg 1995; 52:258± Witte CL, Witte MH, Unger EC, et al Advances in imaging of lymph flow disorders Radiographics 2000; 20:1697±1719 A comprehensive review of the modalities currently in place to examine lymphatics and lymph flow 7 Dreyer G, Noroes J, Figueredo-Silva J, Piessens WF Pathogenesis of lymphatic disease in bancroftian filariasis: a clinical perspective Parasitol Today 2000; 16:544±548 An important exposition of the clinical data suggesting that the adult worm induces lymphatic dysfunction and lymphangiectasia and that several important cofactors are required to induce the severe and chronic disease associated with lymphatic filariasis Beautiful illustrations of clinical pathology are also shown 8 Morel CM Reaching maturity: 25 years of the TDR Parasitol Today 2000; 16:522±528 9 Smith HL, Paciorkowski N, Babu S, Rajan TV Development of a serum-free system for the in vitro cultivation of Brugia malayi infective-stage larvae Exp Parasitol 2000; 95:253±264 An important methodological advance that may allow for a more detailed understanding of early parasite development 10 Smith HL Investigating development of infective stage larvae of filarial nematodes Front Biosci 2000; 5:E95±E Williams SA, Lizotte-Waniewski MR, Foster J, et al The filarial genome project: analysis of the nuclear, mitochondrial and endosymbiont genomes of Brugia malayi Int J Parasitol 2000; 30:411±419 An extremely important update on the filarial genome project as well as the status of the mitochondrial and Wolbachia genomes of B malayi This provides a framework for studies of sequencing the entire Brugia and Wolbachia genomes 12 Fadiel A, Lithwick S, Wanas MQ, Cuticchia AJ Influence of intercodon and base frequencies on codon usage in filarial parasites Genomics 2001; 74:197± Degrave WM, Melville S, Ivens A, Aslett M Parasite genome initiatives Int J Parasitol 2001; 31:531± Underwood AP, Supali T, Wu Y, Bianco AE Two microsatellite loci from Brugia malayi show polymorphisms among isolates from Indonesia and Malaysia Mol Biochem Parasitol 2000; 106:299±302 Microsatellite loci have been identified and used to demonstrate polymorphisms among related parasite isolates 15 Harris MT, Lai K, Arnold K, et al Chitin synthase in the filarial parasite, Brugia malayi Mol Biochem Parasitol 2000; 111:351± Rao UR, Salinas G, Mehta K, Klei TR Identification and localization of glutathione S-transferase as a potential target enzyme in Brugia species Parasitol Res 2000; 86:908± Zang X, Atmadja AK, Gray P, et al The serpin secreted by Brugia malayi microfilariae, Bm-SPN-2, elicits strong, but short-lived, immune responses in mice and humans J Immunol 2000; 165:5161± Vasu C, Reddy MV, Harinath BC A 43-kDa circulating filarial antigen fraction of Wuchereria bancrofti in immunoprophylaxis against Brugia malayi in jirds Parasitol Int 2000; 48:281± Gregory WF, Atmadja AK, Allen JE, Maizels RM The abundant larval transcript- 1 and -2 genes of Brugia malayi encode stage-specific candidate vaccine antigens for filariasis Infect Immun 2000; 68:4174±4179 The identification and molecular characterization of two important larval transcripts and their ability to induce protective immunity in a permissive animal model 20 Manoury B, Gregory WF, Maizels RM, Watts C Bm-CPI-2, a cystatin homolog secreted by the filarial parasite Brugia malayi, inhibits class II MHC-restricted antigen processing Curr Biol 2001; 11:447±451 Identification of a parasite-encoded and secreted cysteine protease inhibitor that inhibits antigen processing Implications for evasion of the host immune response or of its modulation is discussed
6 544 Tropical and travel-associated diseases 21 Gomez-Escobar N, Gregory WF, Maizels RM Identification of tgh-2, a filarial nematode homolog of Caenorhabditis elegans daf-7 and human transforming growth factor beta, expressed in microfilarial and adult stages of Brugia malayi Infect Immun 2000; 68:6402± Krishnamoorthy B, Narayanan K, Miyamoto S, Balakrishnan A Epithelial cells release proinflammatory cytokines and undergo c-myc-induced apoptosis on exposure to filarial parasitic sheath protein-bcl2 mediates rescue by activating c-h-ras In Vitro Cell Dev Biol Anim 2000; 36:532± Dissanayake S Upregulation of a raf kinase and a DP-1 family transcription factor in epidermal growth factor (EGF) stimulated filarial parasites Int J Parasitol 2000; 30:1089± Kozek WJ, Marroquin HF, Brattig NW, et al Intracytoplasmic bacteria in Onchocerca volvulus Am J Trop Med Hyg 1977; 26:663± McLaren DJ, Worms MJ, Laurence BR, et al Micro-organisms in filarial larvae (Nematoda) Trans R Soc Trop Med Hyg 1975; 69:509± Molyneux DH, Taylor MJ Current status and future prospects of the Global Lymphatic Filariasis Programme Curr Opin Infect Dis 2001; 14:155± Hoerauf A, Mand S, Adjei O, et al Depletion of Wolbachia endobacteria in Onchocerca volvulus by doxycycline and microfilaridermia after ivermectin treatment Lancet 2001; 357:1415±1416 Demonstration again of doxycycline's efficacy in eliminating Wolbachia endobacteriae in adult worms of Onchocerca volvulus Sustained absence of microfiladermia after ivermectin treatment provides evidence for the long-term benefit of therapy directed against the filarial endosymbiont 28 Casiraghi M, Anderson TJ, Bandi C, et al A phylogenetic analysis of filarial nematodes: comparison with the phylogeny of Wolbachia endosymbionts Parasitology 2001; 122:93± Taylor MJ, Bandi C, Hoerauf AM, Lazdins J Wolbachia bacteria of filarial nematodes: a target for control? Parasitol Today 2000; 16:179± Townson S, Hutton D, Siemienska J, et al Antibiotics and Wolbachia in filarial nematodes: antifilarial activity of rifampicin, oxytetracycline and chloramphenicol against Onchocerca gutturosa, Onchocerca lienalis and Brugia pahangi Ann Trop Med Parasitol 2000; 94:801± Taylor MJ Wolbachia bacteria of filarial nematodes in the pathogenesis of disease and as a target for control Trans R Soc Trop Med Hyg 2000; 94:596± Hoerauf A, Volkmann L, Nissen-Paehle K, et al Targeting of Wolbachia endobacteria in Litomosoides sigmodontis: comparison of tetracyclines with chloramphenicol, macrolides and ciprofloxacin Trop Med Int Health 2000; 5:275± Bazzocchi C, Jamnongluk W, O'Neill SL, et al wsp gene sequences from the Wolbachia of filarial nematodes Curr Microbiol 2000; 41:96± Taylor MJ, Cross HF, Bilo K Inflammatory responses induced by the filarial nematode Brugia malayi are mediated by lipopolysaccharide-like activity from endosymbiotic Wolbachia bacteria J Exp Med 2000; 191:1429±1436 This study provides clear evidence that the brugian endosymbiont when released from the host worm initiates an inflammatory response that is mediated by lipopolysaccharide binding to its receptor It provides the basis for studies examining the role of the endosymbiont in mediating post treatment adverse reactions 35 Sun LV, Foster JM, Tzertzinis G, et al Determination of Wolbachia genome size by pulsed-field gel electrophoresis J Bacteriol 2001; 183:2219± Dreyer G, Noroes J, Addiss D The silent burden of sexual disability associated with lymphatic filariasis Acta Trop 1997; 63:57±60 37 Gyapong M, Gyapong J, Weiss M, Tanner M The burden of hydrocele on men in Northern Ghana Acta Trop 2000; 77:287±294 Study demonstrating the social and economic burden of lymphatic filarial-induced hydroceles in men 38 Bernhard P, Makunde RW, Magnussen P, Lemnge MM Genital manifestations and reproductive health in female residents of a Wuchereria bancroftiendemic area in Tanzania Trans R Soc Trop Med Hyg 2000; 94:409± Ramaiah KD, Vijay Kumar KN Effect of lymphatic filariasis on school children Acta Trop 2000; 76:197± Ramaiah KD, Das PK, Michael E, Guyatt H The economic burden of lymphatic filariasis in India Parasitol Today 2000; 16:251±253 An important review of the economic impact of lymphatic filarial infections in India, probably the country worldwide in which there are the largest number of infected individuals 41 Gyapong JO, Gyapong M, Evans DB, et al The economic burden of lymphatic filariasis in northern Ghana Trop Med Parasitol 1996; 90:39±46 42 Gyapong JO Lymphatic filariasis in Ghana: from research to control Trans R Soc Trop Med Hyg 2000; 94:599± Haddix AC, Kestler A Lymphatic filariasis: economic aspects of the disease and programmes for its elimination Trans R Soc Trop Med Hyg 2000; 94:592± 593 A concise but comprehensive review of the economic impact of lymphatic filariasis and the likely benefits associated with its control 44 Dreyer G, Noroes J, Figueredo-Silva J New insights into the natural history and pathology of bancroftian filariasis: implications for clinical management and filariasis control programmes Trans R Soc Trop Med Hyg 2000; 94:594± Olszewski WL, Jamal S, Manokaran G, et al Skin changes in filarial and nonfilarial lymphoedema of the lower extremities Trop Med Parasitol 1993; 44:40±44 46 Addiss DG, Dreyer G Treatment of lymphatic filariasis In: Tropical medicine: science and practice Nutman TB (editor) London: Imperial College Press; 2000 pp 151±200 Definitive exposition of our current understanding of treatment for the many clinical entities associated with lymphatic filariasis Using objective definitions for the various clinical conditions, the authors set out the indications regimens for treatment 47 Maizels RM, Allen JE, Yazdanbakhsh M Immunology of lymphatic filariasis: current controversies In: Lymphatic filariasis Tropical medicine: science and practice, Vol 1 Nutman TB (editor) London: Imperial College Press; 2000 pp 217± Ravindran B Are inflammation and immunological hyperreactivity necessary for filarial parasite development? Trends Parasitol 2001; 17:70±73 A hypothesis-generating article in which the author provides a model that attempts to explain the immunological differences seen in early infection and those following the onset of patency in human bancroftian filariasis 49 Satapathy AK, Sahoo PK, Babu Geddam JJ, et al Human bancroftian filariasis: loss of patent microfilaraemia is not associated with production of antibodies to microfilarial sheath Parasite Immunol 2001; 23:163± King CL, Connelly M, Alpers MP, et al Transmission intensity determines lymphocyte responsiveness and cytokine bias in human lymphatic filariasis J Immunol 2001; 166:7427±7436 A study from a focus of lymphatic filariasis in Papua New Guinea where prevalences of lymphatic filariasis are among the highest in the world The authors' data provide compelling evidence that transmission intensity may play a much greater role than heretofore given credence in determining the qualitative nature of the cellular human response to filarial antigens 51 Giambartolomei GH, Lasater BL, Villinger F, Dennis VA Diminished expression of the costimulatory ligand CD80 (B71) gene correlates with antigen-specific cellular unresponsiveness in rhesus monkeys with lymphatic filariasis Acta Trop 2001; 78:67±71 This is one of the few non-human primate studies in lymphatic filariasis Using a model of Brugia malayi in the rhesus monkey, the authors expand on their previous work that had demonstrated diminished cellular responses just at the time of patency to show that CD80 mrna expression is diminished in those monkeys with demonstrable antigen-specific unresponsiveness 52 O'Connor RA, Jenson JS, Devaney E NO contributes to proliferative suppression in a murine model of filariasis Infect Immun 2000; 68:6101± Loke P, MacDonald AS, Robb A, et al Alternatively activated macrophages induced by nematode infection inhibit proliferation via cell-to-cell contact Eur J Immunol 2000; 30:2669±2678 An elegant study demonstrating the presence of `alternatively activated' macrophages that appear to inhibit antigen-specific T cell proliferation by a contact dependent mechanism in Brugia infected mice 54 Loke P, MacDonald AS, Allen JE Antigen-presenting cells recruited by Brugia malayi induce Th2 differentiation of naive CD4(+) T cells Eur J Immunol 2000; 30:1127± Mehlotra RK, Hall LR, Haxhiu MA, Pearlman E Reciprocal immunomodulatory effects of gamma interferon and interleukin-4 on filaria-induced airway hyperresponsiveness Infect Immun 2001; 69:1463± Lawrence RA, Allen JE, Gray CA Requirements for in vivo IFN-gamma induction by live microfilariae of the parasitic nematode, Brugia malayi Parasitology 2000; 120 (Pt 6):631± Hoffmann W, Petit G, Schulz-Key H, et al Litomosoides sigmodontis in mice: reappraisal of an old model for filarial research Parasitol Today 2000; 16:387± Paciorkowski N, Porte P, Shultz LD, Rajan TV B1 B lymphocytes play a critical role in host protection against lymphatic filarial parasites J Exp Med 2000; 191:731±736 A clear demonstration of the importance of the B1 subset of lymphocytes in controlling Brugia infection in permissive strains of mice The importance of phosphorylcholine containing antigens in inducing the expansion of these cells is discussed
7 Lymphatic filariasis Nutman Rajan TV, Paciorkowski N Role of B lymphocytes in host protection against the human filarial parasite, Brugia malayi Curr Top Microbiol Immunol 2000; 252:179± Babu S, Ganley LM, Klei TR, et al Role of gamma interferon and interleukin-4 in host defense against the human filarial parasite Brugia malayi Infect Immun 2000; 68:3034± Martin C, Le Goff L, Ungeheuer MN, et al Drastic reduction of a filarial infection in eosinophilic interleukin-5 transgenic mice Infect Immun 2000; 68:3651± Devaney E, Osborne J The third-stage larva (L3) of Brugia: its role in immune modulation and protective immunity Microbes Infect 2000; 2:1363± Hoerauf A, Fleischer B, Walter RD, et al Of filariasis, mice and men Trends Parasitol 2001; 17:4±5 64 Helmy H, Weil GJ, Faris R, et al Human antibody responses to Wuchereria bancrofti infective larvae Parasite Immunol 2000; 22:89±96 65 Mohanty MC, Satapathy AK, Sahoo PK, Ravindran B Human bancroftian filariasis: a role for antibodies to parasite carbohydrates Clin Exp Immunol 2001; 124:54±61 66 Ravindran B, Satapathy AK, Sahoo PK, Babu Geddam JJ Protective immunity in human bancroftian filariasis: inverse relationship between antibodies to microfilarial sheath and circulating filarial antigens Parasite Immunol 2000; 22:633±637 An important examination of the microfilarial surface reactive antibodies and their role in clearance of microfilariae from the circulation 67 Steel C, Ottesen EA, Mohanty MC, et al Evolution of immunologic responsiveness of persons living in an area of endemic bancroftian filariasis: a 17-year follow-up J Infect Dis 2001; 184:73±79 An immunological assessment of individuals followed clinically and immunologically twice with a span of 17 years The information provided suggests that patent infection, even when cleared over decades, has a long-lasting impact on the antigen-specific T cell responses and antifilarial antibodies 68 Ravindran B, Satapathy AK, Das MK, et al Antibodies to microfilarial sheath in Bancroftian filariasis: prevalence and characterization Ann Trop Med Parasitol 1990; 84:607± Ganley L, Babu S, Rajan TV Course of Brugia malayi Infection in C57BL/6J NOS2 +/+ and 7/7 mice Exp Parasitol 2001; 98:35±43 70 Shenoy RK, John A, Hameed S, et al Apparent failure of ultrasonography to detect adult worms of Brugia malayi Ann Trop Med Parasitol 2000; 94:77±82 The difficulty in adapting ultrasonography for adult worm detection in B malayi infection is suggested by the inability to image these parasites in microfilaremic infections 71 More SJ, Copeman DB, Stephenson LS, et al A highly specific and sensitive monoclonal antibody-based ELISA for the detection of circulating antigen in bancroftian filariasis Trop Med Parasitol 1990; 41:403± Weil GJ, Lammie PJ, Weiss N The ICT filariasis test: a rapid format antigen test for diagnosis of bancroftian filariasis Parasitol Today 1997; 13:401± Rao KV, Eswaran M, Ravi V, et al The Wuchereria bancrofti orthologue of Brugia malayi SXP1 and the diagnosis of bancroftian filariasis Mol Biochem Parasitol 2000; 107:71±80 74 Rahman N, Lim BH, Kahairul Anuar A, et al A recombinant antigen-based IgG4 ELISA for the specific and sensitive detection of Brugia malay infection Trans R Soc Trop Med 2001; 95:280±284 Demonstration of the utility of antibodies to a recombinant antigen for the specific diagnosis of brugian infections 75 Kluber S, Supali T, Williams SA, et al Rapid PCR-based detection of Brugia malayi DNA from blood spots by DNA detection test strips Trans R Soc Trop Med Hyg 2001; 95:169± Cox-Singh J, Pomrehn AS, Wolfe ND, et al Sensitivity of the nestedpolymerase chain reaction (PCR) assay for Brugia malayi and significance of `free' DNA in PCR-based assays Int J Parasitol 2000; 30:1177± Fischer P, Supali T, Wibowo H, et al Detection of DNA of nocturnally periodic Brugia malayi in night and day blood samples by a polymerase chain reaction- ELISA-based method using an internal control DNA Am J Trop Med Hyg 2000; 62:291±296 Improved method for the detection of brugian DNA in blood of infected individuals and the demonstration of its utility in daytime bloods of nocturnally periodic strains of B malayi 78 Dissanayake S, Rocha A, Noroes J, et al Evaluation of PCR-based methods for the diagnosis of infection in bancroftian filariasis Trans R Soc Trop Med Hyg 2000; 94:526± Sehri P, Krishnanand G, Gupta A, Mukherjee A Breast filariasis: a case report Indian J Pathol Microbiol 2000; 43:363± Kibbelaar RE, Hol C, Polderman AM, et al Filaria in an axillary lymph node dissection specimen Histopathology 2000; 37:85±86 81 Bansal R, Mehandru S, Goel A, Jain M A 60 year old woman with axillary mass Diagnosis: axillary lymphadenitis: filarial Postgrad Med J 2000; 76:510± Atal P, Choudhury M, Ashok S Coexistence of carcinoma of the breast with microfilariasis Diagn Cytopathol 2000; 22:259± Gupta S, Sodhani P, Jain S, Kumar N Microfilariae in association with neoplastic lesions: report of five cases Cytopathology 2001; 12:120± Shenoy RK, John A, Babu BS, et al Two-year follow-up of the microfilaraemia of asymptomatic brugian filariasis, after treatment with two, annual, single doses of ivermectin, diethylcarbamazine and albendazole, in various combinations Ann Trop Med Parasitol 2000; 94:607± Dunyo SK, Nkrumah FK, Simonsen PE A randomized double-blind placebocontrolled field trial of ivermectin and albendazole alone and in combination for the treatment of lymphatic filariasis in Ghana Trans R Soc Trop Med Hyg 2000; 94:205± Gyapong JO Impact of single-dose ivermectin on community microfilaria load in bancroftian filariasis infection: two years post treatment Trans R Soc Trop Med Hyg 2000; 94:434± Subramanyam Reddy G, Vengatesvarlou N, Das PK, et al Tolerability and efficacy of single-dose diethyl carbamazine (DEC) or ivermectin in the clearance of Wuchereria bancrofti microfilaraemia in Pondicherry, south India Trop Med Int Health 2000; 5:779± Dunyo SK, Nkrumah FK, Simonsen PE Single-dose treatment of Wuchereria bancrofti infections with ivermectin and albendazole alone or in combination: evaluation of the potential for control at 12 months after treatment Trans R Soc Trop Med Hyg 2000; 94:437± Horton J, Witt C, Ottesen EA, et al An analysis of the safety of the single dose, two drug regimens used in programmes to eliminate lymphatic filariasis Parasitology 2000; 121 (suppl):s147±s160 An exhaustive analysis of 17 large, well-controlled studies examining the safety and efficacy of single drug regimens to which albendazole was added 90 Molyneux DH, Neira M, Liese B, Heymann D Lymphatic filariasis: setting the scene for elimination Trans R Soc Trop Med Hyg 2000; 94:589± Ottesen EA The global programme to eliminate lymphatic filariasis Trop Med Int Health 2000; 5:591±594 A balanced examination of the global elimination effort for lymphatic filariasis with emphasis on the additional benefits afforded above and beyond its impact on lymphatic filariasis 92 Schuetz A, Addiss DG, Eberhard ML, Lammie PJ Evaluation of the whole blood filariasis ICT test for short-term monitoring after antifilarial treatment Am J Trop Med Hyg 2000; 62:502± Freedman DO, Plier DA, De Almeida AB, et al Effect of aggressive prolonged diethylcarbamazine therapy on circulating antigen levels in bancroftian filariasis Trop Med Int Health 2001; 6:37±41 Important demonstration of the difficulties encountered following even prolonged antifilarial therapy with the use of sensitive and quantitative measurements of circulating parasite antigen 94 Hoerauf A, Volkmann L, Hamelmann C, et al Endosymbiotic bacteria in worms as targets for a novel chemotherapy in filariasis Lancet 2000; 355:1242±1243 The initial human study demonstrating the ability of antibiotics (doxycycline) to clear adult Onchocerca volvulus of their endosymbiont bacteria 95 Smith HL, Rajan TV Tetracycline inhibits development of the infective-stage larvae of filarial nematodes in vitro Exp Parasitol 2000; 95:265± Haarbrink M, Abadi GK, Buurman WA, et al Strong association of interleukin-6 and lipopolysaccharide-binding protein with severity of adverse reactions after diethylcarbamazine treatment of microfilaremic patients J Infect Dis 2000; 182:564± Theplertboon R, Fleckenstein L, Dzimianski MT, McCall JW Pharmacokinetics of UMF-078, a candidate antifilarial drug, in infected dogs Am J Trop Med Hyg 2000; 62:86±91 98 Khunkitti W, Fujimaki Y, Aoki Y In vitro antifilarial activity of extracts of the medicinal plant Cardiospermum halicacabum against Brugia pahangi J Helminthol 2000; 74:241± Anderson RJ, Bendell DJ, Hooper M, et al Potential transition state phosphoramidate inhibitors of beta-tubulin as antifilarial agents J Pharm Pharmacol 2001; 53:89± Kinnamon KE, Engle RR, Poon BT, et al Anticancer agents suppressive for adult parasites of filariasis in Mongolian jirds Proc Soc Exp Biol Med 2000; 224:45± Cox FE Elimination of lymphatic filariasis as a public health problem Parasitol Today 2000; 16:135
8 546 Tropical and travel-associated diseases 102 Maher D, Ottesen EA The global lymphatic filariasis initiative Trop Doct 2000; 30:178± Gyapong M, Gyapong JO, Owusu-Banahene G Community-directed treatment: the way forward to eliminating lymphatic filariasis as a publichealth problem in Ghana Ann Trop Med Parasitol 2001; 95:77± Yamey G Global alliance launches plan to eliminate lymphatic filariasis BMJ 2000; 320: Dean M At last, the fight against lymphatic filariasis begins Lancet 2000; 355: Dean M Launching a lymphatic filariasis campaign in the Pacific Islands Lancet 2000; 356: Sabesan S, Palaniyandi M, Das PK, Michael E Mapping of lymphatic filariasis in India Ann Trop Med Parasitol 2000; 94:591± Lindsay SW, Thomas CJ Mapping and estimating the population at risk from lymphatic filariasis in Africa Trans R Soc Trop Med Hyg 2000; 94:37±45 Using climate generated risk profiles, the authors provide a set of maps for the distribution of lymphatic filariasis in Africa 109 Sahoo PK, Geddam JJ, Satapathy AK, et al Bancroftian filariasis: prevalence of antigenaemia and endemic normals in Orissa, India Trans R Soc Trop Med Hyg 2000; 94:515± Ramzy RM, Helmy H, el-lethy AS, et al Field evaluation of a rapid-format kit for the diagnosis of bancroftian filariasis in Egypt East Mediterr Health J 2000; 5:880± Srividya A, Lall R, Ramaiah KD, et al Development of rapid assessment procedures for the delimitation of lymphatic filariasis-endemic areas Trop Med Int Health 2000; 5:64± Rudra SK, Chandra G Comparative epidemiological studies on lymphatic filariasis, between tribal and non-tribal populations of Bankura district, West Bengal, India Ann Trop Med Parasitol 2000; 94:365± da Rocha EM, Fontes G, Brito AC, et al Bancroftian filariasis in urban areas of Alagoas State, Northeast Brazil: study in general population Rev Soc Bras Med Trop 2000; 33:545± Rawlins SC, Lammie P, Tiwari T, et al Lymphatic filariasis in the Caribbean region: the opportunity for its elimination and certification Rev Panam Salud Publica 2000; 7:319± Kron M, Walker E, Hernandez L, et al Lymphatic filariasis in the Philippines Parasitol Today 2000; 16:329± Norman RA, Chan MS, Srividya A, et al EPIFIL: the development of an agestructured model for describing the transmission dynamics and control of lymphatic filariasis Epidemiol Infect 2000; 124:529±541 Description of EPIFIL, a revised mathematical model for describing data on transmission of lymphatic filariasis and how control programs might influence these 117 Plaisier AP, Subramanian S, Das PK, et al The LYMFASIM simulation program for modeling lymphatic filariasis and its control Methods Inf Med 1998; 37:97± Ramaiah KD, Radhamani MP, John KR, et al The impact of lymphatic filariasis on labour inputs in southern India: results of a multi-site study Ann Trop Med Parasitol 2000; 94:353± Ramaiah KD, Das PK, Appavoo NC, et al A programme to eliminate lymphatic filariasis in Tamil Nadu state, India: compliance with annual singledose DEC mass treatment and some related operational aspects Trop Med Int Health 2000; 5:842± Dreyer G, Dreyer P Rational for morbidity management in bancroftian filariasis endemic areas Rev Soc Bras Med Trop 2000; 33:217±221 A compelling argument for morbidity control in the campaigns for lymphatic filariasis elimination 121 Seim AR, Dreyer G, Addiss DG Controlling morbidity and interrupting transmission: twin pillars of lymphatic filariasis elimination Rev Soc Bras Med Trop 1999; 32:325± Schlemper BR Jr, Steindel M, Grisard EC, et al Elimination of bancroftian filariasis (Wuchereria bancrofti) in Santa Catarina state, Brazil Trop Med Int Health 2000; 5:848± Horton J Albendazole: a review of anthelmintic efficacy and safety in humans Parasitology 2000; 121 (suppl):s113±s132 A comprehensive review of albendazole's efficacy and safety profile when used in human helminth infection Provides a rationale for its use not only in lymphatic filariasis but also for treatment of intestinal helminths 124 Stephenson LS, Latham MC, Ottesen EA Malnutrition and parasitic helminth infections Parasitology 2000; 121 (suppl):s23±s Brown KR, Ricci FM, Ottesen EA Ivermectin: effectiveness in lymphatic filariasis Parasitology 2000; 121 (suppl):s133±s146 A comprehensive analysis of ivermectin's efficacy and safety profile when used in human lymphatic filariasis Also provides a rationale for its use for concomitant ectoparasite infections 126 Stephenson LS, Latham MC, Ottesen EA Global malnutrition Parasitology 2000; 121 (suppl):s5±s22
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