Dataset

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Title of Dataset
Data from: Identification of Non-HIV Immunogens That Bind to Germline b12 Predecessors and Prime for Elicitation of Cross-clade Neutralizing HIV-1 Antibodies
Author of Dataset
Yang, Zheng1
Li, Jingjing1
Liu, Qingsheng1
Yuan, Tingting1
Zhang, Yanyu1
Chen, Li-Qing2
Lou, Qi2
Sun, Zehua1
Ying, Huazhong2
Xu, Jianqing3
Dimitrov, Dimiter S.4
Contact
Zhang, Mei-Yun5
Date of Dataset Creation
2015-05-27
Description
A fundamental challenge for developing an effective and safe HIV-1 vaccine is to identify vaccine immunogens that can initiate and maintain immune responses leading to elicitation of broadly neutralizing HIV-1 antibodies (bnAbs) through complex maturation pathways. We have previously found that HIV-1 envelope glycoproteins (Env) lack measurable binding to putative germline predecessors of known bnAbs and proposed to search for non-HIV immunogens that could initiate their somatic maturation. Using bnAb b12 as a model bnAb and yeast display technology, we isolated five (poly)peptides from plant leaves, insects, E. coli strains, and sea water microbes that bind to b12 putative germline and intermediate antibodies. Rabbit immunization with the (poly)peptides alone induced high titers of cross-reactive antibodies that neutralized HIV-1 isolates SF162 and JRFL. Priming rabbits with the (poly)peptides followed by boosts with trimeric gp140SF162 and then resurfaced Env (RSC3) induced antibodies that competed with mature b12 and neutralized tier 1 and 2 viruses from clade B, C and E, while control rabbits without (poly)peptide priming induced antibodies that did not compete with mature b12 and neutralized fewer isolates. The degree of competition with mature b12 for binding to gp140SF162 correlated with the neutralizing activity of the rabbit IgG. Reversing the order of the two boosting immunogens significantly affected the binding profile and neutralization potency of the rabbit IgG. Our study is the first to provide evidence that appears to support the concept that non-HIV immunogens may initiate immune responses leading to elicitation of cross-clade neutralizing antibodies.
Citation
Yang, Z, Li, J, Liu, Q, Yuan, T, Zhang, Y, Chen, LQ, Lou, Q, Sun, Z, Ying, H, Xu, J, Dimitrov, DS, Zhang, MY. (2015). Data from: Identification of Non-HIV Immunogens That Bind to Germline b12 Predecessors and Prime for Elicitation of Cross-clade Neutralizing HIV-1 Antibodies. [Data File]. All relevant data are within the paper. Click on “Linked Publications” to access the publication and access supporting information on figshare at https://figshare.com/articles/_Identification_of_Non_HIV_Immunogens_That_Bind_to_Germline_b12_Predecessors_and_Prime_for_Elicitation_of_Cross_clade_Neutralizing_HIV_1_Antibodies_/1426720
Subject (RGC Codes)
M2 — Medicine, Dentistry & Health — 醫學, 牙科學及保健
  • 1206 — Clinical Trials — 臨床試驗
Subject (ANZSRC)
11 — MEDICAL AND HEALTH SCIENCES — 醫學與衛生科學
  • 1108 — MEDICAL MICROBIOLOGY — 醫學微生物學
    • 110802 — Medical Infection Agents (incl. Prions) — 醫學致病因子
Keyword
immunogen
b 12
jrfl
yeast display technology
antibody
sea water microbes
poly
trimeric gp 140SF
neutralizing
Germline b 12 Predecessors
binding
bnAb b 12
rabbit IgG
hiv
rsc
Affiliations
  1. Univ Hong Kong, Li Ka Shing Fac Med, AIDS Inst, Dept Microbiol, Pok Fu Lam, Hong Kong, Peoples R China
  2. Zhejiang Acad Med Sci, Ctr Lab Anim, Shanghai, Zhejiang, Peoples R China
  3. Fudan Univ, Shanghai Publ Hlth Clin Ctr, Inst Biomed Sci, Shanghai 201508, Peoples R China
  4. NCI, Prot Interact Grp, Immunol Lab, Canc & Inflammat Program,Ctr Canc Res,NIH, Frederick, MD 21701 USA
  5. Univ Hong Kong, Li Ka Shing Fac Med, AIDS Inst, Dept Microbiol, Pok Fu Lam, Hong Kong, Peoples R China ; Shenzhen Third Peoples Hosp, Liver Dis Inst, Shenzhen 518112, Peoples R China