Nef protein of HIV-1 has B-cell stimulatory activity
- PMID: 8086129
- DOI: 10.1097/00002030-199406000-00002
Nef protein of HIV-1 has B-cell stimulatory activity
Abstract
Objective: To examine the B-cell stimulatory properties of the regulatory Nef protein of HIV-1.
Methods: The effect of the HIV-1 regulatory proteins Nef, Tat and Vif, were analyzed for their ability to induce differentiation of normal B lymphocytes into immunoglobulin secreting cells (ISC).
Results: A recombinant Nef protein, but neither Tat or Vif, was able to induce ISC in peripheral blood lymphocyte (PBL) cultures of HIV-1-seronegative donors. Another recombinant Nef protein, d-Nef, with a truncated amino terminal (deletion of 34 amino acids) failed to induce B-cell differentiation. Pretreatment of the Nef protein with a polyclonal anti-Nef-antibody abrogated its B-cell stimulatory activity. The Nef-induced B-cell differentiation was dependent on cell-to-cell contact. Cell surface molecules leukocyte function-associated molecule (LFA)-1, intracellular adhesion molecule (ICAM)-1, human lymphocyte antigen-DR and B7 were involved in the T-B-cell interaction because monoclonal antibodies to these molecules abrogated the Nef-induced B-cell differentiation response. The Nef protein was able to induce interleukin (IL)-6 messenger (m)RNA and IL-6 protein secretion in PBL, with monocytes as the primary source.
Conclusions: These findings indicate that regulatory (Nef) proteins of HIV-1 contribute to the intense B-cell activation that occurs in association with HIV-1 infection. T-B-cell contact-dependent interaction and induction of IL-6 by these proteins appear to play major roles in this process.
Similar articles
-
HIV-1 Nef protein inhibits the in vitro induction of a specific antibody response to Candida albicans by an early up-regulation of IL-15 production.Clin Exp Immunol. 2000 Dec;122(3):358-63. doi: 10.1046/j.1365-2249.2000.01388.x. Clin Exp Immunol. 2000. PMID: 11122241 Free PMC article.
-
HIV-gp 160-induced T cell-dependent B cell differentiation. Role of T cell-B cell activation molecule and IL-6.J Immunol. 1993 Mar 15;150(6):2478-86. J Immunol. 1993. PMID: 8450224
-
Antibodies to recombinant HIV-1 vif, tat, and nef proteins in human sera.Med Microbiol Immunol. 1990;179(1):1-11. doi: 10.1007/BF00190145. Med Microbiol Immunol. 1990. PMID: 2184337
-
Human immune response to HIV-1-Nef. I. CD45RO- T lymphocytes of non-infected donors contain cytotoxic T lymphocyte precursors at high frequency.Int Immunol. 1994 Nov;6(11):1739-49. doi: 10.1093/intimm/6.11.1739. Int Immunol. 1994. PMID: 7865467
-
How T-lymphocytes are activated and become activators by cell-cell interaction.Eur Respir J Suppl. 2003 Sep;44:10s-15s. doi: 10.1183/09031936.03.00000403b. Eur Respir J Suppl. 2003. PMID: 14582893 Review. No abstract available.
Cited by
-
Positive selection of HIV host factors and the evolution of lentivirus genes.BMC Evol Biol. 2010 Jun 18;10:186. doi: 10.1186/1471-2148-10-186. BMC Evol Biol. 2010. PMID: 20565842 Free PMC article.
-
Acquisition of host-derived CD40L by HIV-1 in vivo and its functional consequences in the B-cell compartment.J Virol. 2011 Mar;85(5):2189-200. doi: 10.1128/JVI.01993-10. Epub 2010 Dec 22. J Virol. 2011. PMID: 21177803 Free PMC article.
-
Interleukin 10 is induced by recombinant HIV-1 Nef protein involving the calcium/calmodulin-dependent phosphodiesterase signal transduction pathway.Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3178-82. doi: 10.1073/pnas.94.7.3178. Proc Natl Acad Sci U S A. 1997. PMID: 9096366 Free PMC article.
-
Nef defect attenuates HIV viremia and immune dysregulation in the bone marrow-liver-thymus-spleen (BLTS) humanized mouse model.Virology. 2024 Oct;598:110192. doi: 10.1016/j.virol.2024.110192. Epub 2024 Jul 31. Virology. 2024. PMID: 39106585 Free PMC article.
-
Envelope glycoproteins of human immunodeficiency virus type 1: profound influences on immune functions.Microbiol Rev. 1996 Jun;60(2):386-406. doi: 10.1128/mr.60.2.386-406.1996. Microbiol Rev. 1996. PMID: 8801439 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous