Relevant Communicable Diseases in HCT/Ps

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Relevant Communicable Diseases in HCT/Ps Phyllis I. Warkentin, MD Professor of Pathology and Pediatrics University of Nebraska Medical Center FACT Chief Medical Officer

Relevant Communicable Diseases in HCT/Ps ZIKA Virus HCT/Ps derived from peripheral blood, bone marrow Cord blood West Nile Virus Other arthropod-borne viruses Dengue, Chikungunya Similar challenges: asymptomatic viremia; likely transmissible; lack of approved test Various geographic distributions

ZIKA Virus RNA flavivirus transmitted by various Aedes species mosquitoes Clinical Disease: Associated with neurologic manifestations; Guillain-Barré syndrome Associated with birth defects [microcephaly] in newborns 80% of infected individuals are asymptomatic Viremia 10 days or more after symptoms Also in saliva, urine, breast milk, semen [62 d; 10 weeks] Transmission: Sexual transmission [male to female] Transfusion Gestational tissues: amniotic membrane/fluid; placenta; cord blood Relevant communicable disease agent under 21 CFR 1271.3 [GUIDANCE FOR INDUSTRY, March 2016]

HCT/P Donor Eligibility March 2016 HCT/P Guidance: Donor ineligible if Medical diagnosis of ZIKV infection 6 months Residence in or travel to area active ZIKV transmission Sex in past 6 months with male with either risk factor If not possible to determine [3 above] = incomplete Confusion exists regarding how to label product if ZIKV assessment incomplete Ineligible for another reason: [lived in Europe or UK; +HBc]

HCT/P Donor Eligibility Under the unified tiered approach to HCT/P regulation, all HCT/Ps are regulated together Different HCT/Ps may have different communicable disease risk based on source of cells and disease agent HPC, Apheresis products from normal volunteer donors similar to other apheresis-derived blood components: Low risk donor population Method of collection Actual tissue components present in end product

HCT/P Donor Eligibility August 2016 Guidance allows testing of volunteer blood donors with investigational test for ZIKA virus Such testing not permitted for HPC, Apheresis donors due to all HCT/Ps regulated together Result is more ineligible donors [6 month deferral/ ineligibility] Decisions based upon presumed risk and clinical need Is there consideration to treat the apheresis-derived HCT/Ps more like apheresis platelets for this assessment of eligibility?

ZIKA Virus / Cord Blood Strong association between risk of microcephaly and first trimester ZIKV infection; negligible in second and third trimester Recent studies association between ZIKV infection in any trimester and adverse pregnancy outcome Little is known about effects of mild or asymptomatic ZIKV infections at any time, or of infections in early pregnancy - women may be unaware of pregnancy

ZIKA Virus / Cord Blood Challenge to CBB: Can exclude clearly affected infants or symptomatic mothers Residence in area of active transmission at any time 6 months pre-pregnancy through entire pregnancy make donor ineligible? Cord blood banking in Latin America is rapidly growing Snapshot of accredited cord blood banks: FLORIDA BRAZIL SINGAPORE PANAMA FACT-NetCord 3 1 3 AABB 4 3 1

ZIKA Virus / Cord Blood CBB affiliated with NMDP also report potential issues with decreased collections and bankable units July 2016 survey; 17 CBB respondents Various methods of regulatory compliance Negative impact on the national inventory of CB units Is there a potential to utilize a test under IND for either the maternal samples, the stored maternal samples, or stored cord blood unit samples? Selected products with travel history / residence only [no symptomatic disease]

West Nile Virus

West Nile Virus Endemic in the United States First recognized in US in 1999 Outbreaks of disease recognized annually Mosquitoes that transmit are present in US Human to human transmission well documented Asymptomatic illnesses Universal donor screening available and used On-going research: Genetic variability and mutation Impact on virulence Variants escape detection; need to maintain relevant reagents Potential approachs to increase sensitivity of current assays

West Nile Virus West Nile Virus is a relevant communicable disease HCT/P donors screened / tested within 30 days of collection Day of collection testing eliminated by registries Probably most valuable test, but not useful products already infused FDA Guidance [2007; referenced 9/2016] persons who have tested positive in the preceding 120 days should be considered ineligible FDA Guidance [09/2016] Any HCT/P donor with a negative test should be considered to be negative for WNV for eligibility determination.

West Nile Virus Is there specific guidance related to time frame required since last positive test to call a donor eligible? How long is the period of ineligibility after a positive test?

Thank you