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Tissue memory B cell repertoire analysis after ALVAC/AIDSVAX B/E gp120 immunization of rhesus macaques
Kan Luo, … , Barton F. Haynes, M. Anthony Moody
Kan Luo, … , Barton F. Haynes, M. Anthony Moody
Published December 8, 2016
Citation Information: JCI Insight. 2016;1(20):e88522. https://doi.org/10.1172/jci.insight.88522.
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Research Article AIDS/HIV Vaccines

Tissue memory B cell repertoire analysis after ALVAC/AIDSVAX B/E gp120 immunization of rhesus macaques

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Abstract

The ALVAC prime/ALVAC + AIDSVAX B/E boost RV144 vaccine trial induced an estimated 31% efficacy in a low-risk cohort where HIV‑1 exposures were likely at mucosal surfaces. An immune correlates study demonstrated that antibodies targeting the V2 region and in a secondary analysis antibody-dependent cellular cytotoxicity (ADCC), in the presence of low envelope-specific (Env-specific) IgA, correlated with decreased risk of infection. Thus, understanding the B cell repertoires induced by this vaccine in systemic and mucosal compartments are key to understanding the potential protective mechanisms of this vaccine regimen. We immunized rhesus macaques with the ALVAC/AIDSVAX B/E gp120 vaccine regimen given in RV144, and then gave a boost 6 months later, after which the animals were necropsied. We isolated systemic and intestinal vaccine Env-specific memory B cells. Whereas Env-specific B cell clonal lineages were shared between spleen, draining inguinal, anterior pelvic, posterior pelvic, and periaortic lymph nodes, members of Env‑specific B cell clonal lineages were absent in the terminal ileum. Env‑specific antibodies were detectable in rectal fluids, suggesting that IgG antibodies present at mucosal sites were likely systemically produced and transported to intestinal mucosal sites.

Authors

Kan Luo, Hua-Xin Liao, Ruijun Zhang, David Easterhoff, Kevin Wiehe, Thaddeus C. Gurley, Lawrence C. Armand, Ashley A. Allen, Tarra A. Von Holle, Dawn J. Marshall, John F. Whitesides, Jamie Pritchett, Andrew Foulger, Giovanna Hernandez, Robert Parks, Krissey E. Lloyd, Christina Stolarchuk, Sheetal Sawant, Jessica Peel, Nicole L. Yates, Erika Dunford, Sabrina Arora, Amy Wang, Cindy M. Bowman, Laura L. Sutherland, Richard M. Scearce, Shi-Mao Xia, Mattia Bonsignori, Justin Pollara, R. Whitney Edwards, Sampa Santra, Norman L. Letvin, James Tartaglia, Donald Francis, Faruk Sinangil, Carter Lee, Jaranit Kaewkungwal, Sorachai Nitayaphan, Punnee Pitisuttithum, Supachai Rerks-ngarm, Nelson L. Michael, Jerome H. Kim, S. Munir Alam, Nathan A. Vandergrift, Guido Ferrari, David C. Montefiori, Georgia D. Tomaras, Barton F. Haynes, M. Anthony Moody

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Figure 4

Characteristics of isolated HIV-1 envelope–reactive mAbs.

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Characteristics of isolated HIV-1 envelope–reactive mAbs.
There were 1,4...
There were 1,493 mAbs isolated of which 1,242 were reactive with HIV‑1 antigens during screening. (A) For rhesus macaque (RM) 22‑11, mAbs were isolated only from peripheral blood mononuclear cells (PBMCs). For RMs 66‑11 and 60‑11, envelope-reactive (Env-reactive) mAbs were isolated from most tissue compartments. (B) The majority (95%) of isolated mAbs were of IgG isotype. (C) VH gene segment usage was similar among the RMs with the majority of mAbs using VH1, VH3, and VH4. Overall, 55% of mAbs used lambda chains. For kappa chain–using mAbs, the majority used Vκ1/1D or Vκ2/2D (D); for lambda chain–using mAbs, the majority used Vλ1, Vλ2, or Vλ3 (E). Each animal had some Env-reactive mAbs that used Vλ3~17, the lambda chain associated with genetically conserved V1V2 responses. (F) Heavy chain (HC) mutation frequencies were similar among Env-reactive antibodies for all 3 RMs; the overall mean mutation frequency was 9.3%.

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