Walker: bNabs after Infection and Immunization
The development of a safe and effective HIV vaccine is the final missing piece in the complex puzzle of how to attain affordable, durable control of the HIV/AIDS pandemic. At present there are promising leads, but no clear and unequivocal path, to the development of an HIV vaccine. It is likely that the field will have to overcome the key challenge of eliciting a broad neutralizing antibody response in the majority of vaccinated individuals, but so far, candidate HIV vaccines have not elicited any significant levels of broadly neutralizing antibodies (bNabs). This grant directly addresses the neutralizing antibody problem using innovative technology that may be transformative in the quest for an HIV vaccine.
By stepping back from the problem and taking a comprehensive and unbiased look at how broad neutralizing activity arises in the approximately 25% of HIV-infected individuals who do develop it, this grant proposes to efficiently learn the circumstances under which bNabs are elicited, and, correspondingly, what vaccines need to do to elicit them. The project will be anchored by technology developed by Atreca, Inc., which represents a powerful, high-throughput, unbiased approach to understanding the antibody response to infection and vaccination. The earliest B-cell responses in HIV infection, including those active just before infection, will be studied and followed prospectively for up to three years in human volunteers who face an exceptionally high rate of HIV infection in KwaZulu-NatalZN, South Africa, along with other cohorts with more immediately available samples. The study in South Africa (called "FRESH") will be unique in its capacity to enroll and follow volunteers twice-weekly with a finger-stick blood sample, permitting ascertainment of HIV infection as soon as any trace of the virus is detectable in the bloodstream. Evaluation of the status of the B-cell response before infection, during the first days and weeks of infection, and for the next 2-3 years will be enabled, and the follow-up period will allow identification of those who do and do not go on to develop broad neutralizing activity. For this work the researchers have defined broad neutralizing activity as a continuum, ranging from neutralization of only the infecting virus strain (called autologous neutralization) at one end, and equivalent to the very best broadly neutralizing antibodies (bNabs) at the other, in order to capture all stages of bNab development. Moreover, the study will include a broader assessment of innate and adaptive immunity, building up a complex of immune data that will provide important context for understanding the factors that support bNab development. It represents a significant step away from a purely empirical approach to HIV vaccines.
This consortium is led by Bruce Walker, a leading HIV researcher who excels at assembling informative cohorts for studies of immune protection against HIV. A team of investigators from the Ragon Institute of MGH, MIT, and Harvard, will join with investigators from the University of KwaZulu- Natal (SA) and Atreca, to conduct different aspects of the study.
1. To collect longitudinal samples from individuals with acute HIV-1 infection to investigate the development of broad neutralizing responses
2. To define the B-cell signatures associated with the induction of HIV-specific neutralizing antibodies using the Atreca technology and other measures of B-cell development and maturation
3. To define the HIV-specific CD4+ T-cell responses and their relationship to the establishment of broad neutralizing responses
4. To identify transcriptional signatures of HIV-specific broad neutralizing activity using a systems biology approach applied to relevant cell subsets of the immune system
5. To obtain large volume blood samples for characterizing the parameters associated with breadth of neutralizing antibodies in HIV controllers with different degrees of antigen load and diversity, and with relatively good preservation of immune function
The FRESH Cohort (Females Rising through Education, Support and Health) of women at high risk for HIV infection has been recruited in KwaZulu-Natal
Province, South Africa, and is well on its way to a goal of enrolling 300 women by the end of 2013. A newly renovated clinic site at a shopping mall has been established, where each participant is seen twice weekly and given classes designed to empower them by teaching life skills, job skills, and help with obtaining a high school degree. Each time the participants come in they also have a finger prick blood draw looking for acute HIV infection. Incidence of infection is running about 8% per year, and pre and post-infection blood samples are being obtained for studies of the ontogeny of neutralizing antibodies.
Additional cohorts of persons with acute infection are being recruited in Berlin and leukapheresis and whole bloods draws are being obtained from a cohort of elite controllers both with and without broadly neutralizing antibodies in the United States.
Longitudinal and cross-sectional studies of the CD4 T cell and B cell signatures associated with the development of broadly neutralizing antibodies have been initiated, and cell subsets have been isolated for evaluation of transcriptional signatures of HIV specific broadly neutralizing antibodies.
The BCR repertoire of both antigen-specific memory B cells and plasmablasts has already been generated by Atreca on eight spontaneous controllers who exhibit broad neutralizing antibody responses. Preliminary studies on 16 monoclonal antibodies generated from the first three sequenced subjects showed antigen specificity and neutralizing capacity. Cutting edge BCR computational tools for BCR analysis, linked to the generation of novel selection criteria are being utilized to maximize the selection of sets of new mAbs from broad neutralizers to gain deeper insights into the pathways and mechanisms by which neutralizing B cell responses are selected.