BIOE 301. Summary. Lecture Ten. Vaccine Trials in the News Ebola. Vaccine Trials in the News HIV. HIV Vaccine pre-clinical trials 2010

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Summary BIOE 301 Lecture Ten How do vaccines work? Stimulate immunity without causing disease How are vaccines made? Non-infectious vaccines Live, attenuated bacterial or viral vaccines Carrier Vaccines DNA Vaccines How are vaccines tested? Lab/Animal testing Phase I-III human testing Post-licensure surveillance Impact of vaccines Vaccine Trials in the News Ebola 2003 pre-clinical trials 2010 New species of Ebola - Bundibugyo - emerged in 2007 Experimental vaccines being developed against other lethal Ebola species found to totally protected against it did not stimulate antibodies against the new species protection depended entirely on cellular immunity "The dogma is that viruses require an antibody response to prevent the virus from entering the cell," Sullivan says. "This is truly the first time that cell-mediated immunity alone has been shown to be protective against virus infection. Vaccine Trials in the News Ebola Study Design 8 macaques 4 vaccinated / 4 unvaccinated All inoculated with lethal doses of Ebola Vaccinated animals survived, Unvaccinated animals died Vaccine pieces of the Zaire & Sudan viruses protein-sugar coat (glycoprotein) inserted into a type of common cold virus The cold virus carries the Ebola glycoprotein into cells of the vaccine recipients 4 "priming" shots, followed a year later with a booster There's no way to do trials of Ebola vaccines in humans. Unlike, say, a vaccine for HIV, there's no identifiable group of people at risk for Ebola... Vaccine Trials in the News HIV 2009: 3 rd largest AIDS vaccine trial to date Cost the US government $105 M Largest done in humans: >16,000 participants Controversy: Combination of 2 vaccines that each failed when tested for use individually 2004 editorial in Science signed by 22 top AIDS researchers: Suggested trial was a waste of $$ NPR: AIDS Vaccine Prevents Some HIV Infections Vaccines Tested: Sanofi-Aventis Alvac-HIV Carrier vaccine Canarypox virus with 3 AIDS virus genes grafted onto it Stimulate cell mediated immunity Genentech Aidsvax Non-infectious sub-unit vaccine Contains two recombinant gp120 proteins found on surface of different strains of HIV virus Stimulate anti-body mediated immunity

Study Design Followed 16,402 Thai volunteers Men & women, ages 18-30 Recruited from general population Half got six doses of combination of two different vaccines Half got placebo Followed for 3 years Ethics: All were offered condoms Taught how to avoid infection Promised lifelong ARVs if infected Results: Placebo group: 74 infected Vaccinated group: 51 infected Vaccine Effectiveness Effect size: 23 people of >16,000 From ~0.9% to ~0.6% incidence A 31% decrease 1 st time any protective effect observed Conclusions: Studies to be done to understand why worked What is unique about those it worked in? Through what mechanism did it work?! Why those vaccinated who become HIV+ didn t develop any protective effect? Those who became infected have as much virus in blood whether they got vaccine or placebo Suggests vaccine does not produce neutralizing Abs Dangers of Vaccine Trials Most researchers feel first HIV vaccines will not be more than 40-50% effective Will vaccinated individuals engage in higher risk behaviors? Vaccine could cause as much harm as it prevents http://www.npr.org/templates/story/story.php?storyid=113177004 Future vaccines cannot be tested against placebo, would be unethical In-Class Activity Town Hall Meeting A Ugandan community has been asked to participate in a clinical trial of an HIV vaccine 10 volunteers to role play, 3 Ugandan council members & 7 experts both for & against Remaining students represent the community making the decision to participate or not One by one volunteers explain their stance Audience may ask questions at any time Does the community choose to participate?

Ethics of Clinical Research Humans have not always treated each other humanely in the name of science Ethics of Clinical Research Famous Case Studies Codes governing ethical conduct of research: Nuremberg Code Belmont Report Case Studies Revisited Functions of the IRB Applications to current controversies Goal: Examine natural history of untreated syphilis 400 black men with syphilis Half to receive standard Rx Half to be left untreated 200 normal controls 1932: Standard Rx: injection of compounds containing heavy metals Treatment reduced mortality but heavy metals thought to cause syphilis complications Treatment withheld from infected men 1942: Death rate 2X higher in treatment group 1940s: Penicillin available Men not informed of this Study continued until 1972 when first publicized Consent Process: No informed consent Men misinformed that some study procedures (spinal taps) were free extra treatment Case II: Willowbrook Studies Goal: Understand natural history of infectious hepatitis Children at Willowbrook State School An institution for mentally defective persons Carried out from 1963-1966 Subjects deliberately infected with hepatitis Fed extracts of stool from infected persons Injected with purified virus Vast majority of children admitted acquired hepatitis Case II: Willowbrook Studies Consent Process Parents gave consent Due to crowding, Willowbrook was at times closed to new patients Hepatitis project had its own space In some cases, only way to gain admission was to participate in the study

Case III: Jewish Chronic Disease Hospital Study Goal: Study rejection of cancer cells Healthy patients reject cancer cell implants quickly Cancer patients reject cancer cell implants much more slowly Is this due to decreased immunity because of presence of cancer or is it manifestation of debility? Patients hospitalized with various chronic debilitating diseases Took place in 1963 Patients injected with live liver cancer cells Case III: Jewish Chronic Disease Hospital Study Consent Process: Negotiated orally, but not documented Patients not told that cancer cells would be injected because this might scare them unnecessarily Investigators justified this because they were reasonably certain the cancer cells would be rejected Case IV: San Antonio Contraceptive Study Goal: Which side effects of OCP are due to drug? Which are by-products of every-day life? 76 Impoverished Mexican-American women with previous multiple pregnancies Patients had come to a public clinic seeking contraceptive assistance. Case IV: San Antonio Contraceptive Study Took place in the 1970s Randomized, double-blind, placebo controlled trial Cross-over design All women were instructed to use vaginal cream as contraceptive during the study 11 women became pregnant during study, 10 while using placebo Consent Process: None of the women were told study involved placebo Nuremberg Code: 1949 Voluntary consent of the human subject is absolutely essential Experiment should yield fruitful results for good of society, obtainable in no other way Experiments should avoid all unnecessary mental and physical suffering No experiment should be performed if it is believed that death or disabling injury may occur Belmont Report: 1979 From Dept. of Health, Education & Welfare Statement of: Basic ethical principles and guidelines to resolve ethical problems associated with conduct of research with human subjects Three basic ethical principles:

Belmont Report: What is research? Clinical Practice: Interventions designed solely to enhance well-being of an individual patient that have a reasonable expectation of success Research: An activity to test a hypothesis Permit conclusions to be drawn Contribute to generalizable knowledge Usually described in formal protocol that sets forth an objective and procedures to reach that objective Respect for Persons All individuals should be treated as autonomous agents Demands that subjects enter into research: Voluntarily With enough information to make a decision Persons with diminished autonomy are entitled to special protection Prisoners Children Beneficence Make efforts to secure patients well-being Do No Harm Maximize possible benefits Minimize possible harms One should not injure one person regardless of benefits that may come to others Justice Who should receive benefits of research and who should bear its burdens? Some ways to distribute burdens & benefits: To each person an equal share To each person according to individual need To each person according to individual effort 19 th Century: Poor ward patients were research subjects Wealthy private patients received benefits of research Selection of research subjects must be scrutinized: Are some classes are being selected because of easy availability, compromised position or manipulability. Application of Belmont Report Informed Consent Assessment of Risks and Benefits Selection of Subjects Informed Consent Information: Research procedure, purpose of study, risks and anticipated benefits, alternative procedures, statement offering subject opportunity to withdraw at any time Comprehension: Must present information in a way subject can understand Must not be disorganized, too rapid, above subject s educational level Voluntariness: Consent must be given voluntarily Persons in positions of authority cannot urge course of action

Assessment of Risks & Benefits Research must be justified based on favorable risk/benefit assessment Risk: Possibility that harm may occur Brutal or inhumane treatment of subjects is never morally justified Risks should be reduced to those necessary to achieve research objective Benefit: Positive value related to health or welfare Selection of Subjects Individual Justice: Researchers must select subjects fairly Must not select only potentially beneficial research to some subjects in their favor Must not select only undesirable persons for risky research. Social Justice: Distinctions be drawn between classes that ought and ought not to participate in research based on ability of that class to bear burdens Adults before children Case II: Willowbrook Studies 1997: President Clinton formally apologizes to subjects of the study http://www.npr.org/programs/morning/featur es/2002/jul/tuskegee/ Case III: Jewish Chronic Disease Hospital Study Case IV: San Antonio Contraceptive Study

Role of IRB Work with investigators to be sure that the rights of subjects are protected Educate research community and public about ethical conduct of research Resource centers for information about Federal guidelines Not a police force Real Controversies Egg Donation http://www.eggdonor.com http://www.npr.org/templates/story/story.php?storyi d=5035034 Life Threatening Situations http://www.npr.org/templates/story/story.php?storyi d=1045001 Terminally Ill Patients