| Literature DB >> 25121750 |
Ashley M Trama1, M Anthony Moody2, S Munir Alam3, Frederick H Jaeger3, Bradley Lockwood3, Robert Parks3, Krissey E Lloyd3, Christina Stolarchuk3, Richard Scearce3, Andrew Foulger3, Dawn J Marshall3, John F Whitesides3, Thomas L Jeffries3, Kevin Wiehe3, Lynn Morris4, Bronwen Lambson4, Kelly Soderberg3, Kwan-Ki Hwang3, Georgia D Tomaras5, Nathan Vandergrift3, Katherine J L Jackson6, Krishna M Roskin6, Scott D Boyd6, Thomas B Kepler7, Hua-Xin Liao3, Barton F Haynes8.
Abstract
Monoclonal antibodies derived from blood plasma cells of acute HIV-1-infected individuals are predominantly targeted to the HIV Env gp41 and cross-reactive with commensal bacteria. To understand this phenomenon, we examined anti-HIV responses in ileum B cells using recombinant antibody technology and probed their relationship to commensal bacteria. The dominant ileum B cell response was to Env gp41. Remarkably, a majority (82%) of the ileum anti-gp41 antibodies cross-reacted with commensal bacteria, and of those, 43% showed non-HIV-1 antigen polyreactivity. Pyrosequencing revealed shared HIV-1 antibody clonal lineages between ileum and blood. Mutated immunoglobulin G antibodies cross-reactive with both Env gp41 and microbiota could also be isolated from the ileum of HIV-1 uninfected individuals. Thus, the gp41 commensal bacterial antigen cross-reactive antibodies originate in the intestine, and the gp41 Env response in HIV-1 infection can be derived from a preinfection memory B cell pool triggered by commensal bacteria that cross-react with Env.Entities:
Mesh:
Substances:
Year: 2014 PMID: 25121750 PMCID: PMC4294419 DOI: 10.1016/j.chom.2014.07.003
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023