Production and characterization of SIV envelope-specific rhesus monoclonal antibodies from a macaque asymptomatically infected with a live SIV vaccine. NLM AIDSLINE Important note: Information in this article was accurate in 1999. The state of the art may have changed since the publication date.

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Production and characterization of SIV envelope-specific rhesus monoclonal antibodies from a macaque asymptomatically infected with a live SIV vaccine.

AIDS Res Hum Retroviruses. 1998 Sep 20;14(14):1253-62. Unique Identifier : AIDSLINE MED/98435938
Robinson JE; Cole KS; Elliott DH; Lam H; Amedee AM; Means R; Desrosiers RC; Clements J; Montelaro RC; Murphey-Corb M; Department of Pediatrics, Tulane University Medical School, New; Orleans, Louisiana 70112, USA.


Abstract: Five rhesus monoclonal antibodies (RhMAbs) were produced by rhesus EBV transformation of peripheral blood B cells from a rhesus macaque that had been asymptomatically infected with an attenuated, macrophage-tropic SIV strain, 17E-Cl. These MAbs recognized conformation-dependent epitopes on SIV gp120 and could not be mapped using synthetic peptides. All five RhMAbs were able to neutralize the vaccine strain and a heterologous isolate, SIV/DeltaB670. The RhMAbs did not cross-react with HIV-2; by contrast, four human MAbs derived from an HIV-2-infected person were broadly cross-reactive with both SIV and HIV-2 gp120s. Cross-competition analysis indicated that the five RhMAbs could be placed in two groups recognizing two nonoverlapping epitopes; while the HMAbs were placed in two additional competition groups. Binding of the three group I RhMAbs (1.7F, 3.11B, and 1.10A) as well as HMAb 17A was shown to be sensitive to specific amino acid alterations in V4 occurring in natural env variants. The results of this study demonstrate that RhEBV transformation provides a means to probe rhesus antibody responses to SIV infection at the monoclonal level. RhMAbs will allow structural and functional studies of envelope glycoprotein determinants that elicit protective immune responses against SIV.
Keywords: JOURNAL ARTICLE Amino Acid Sequence Animal Antibodies, Monoclonal/BIOSYNTHESIS/*IMMUNOLOGY Base Sequence Binding, Competitive Blotting, Western Cross Reactions Fluorescent Antibody Technique Human HIV Envelope Protein gp120/IMMUNOLOGY HIV-2/IMMUNOLOGY Immunoenzyme Techniques Macaca mulatta/*IMMUNOLOGY Molecular Sequence Data Neutralization Tests Peptide Mapping Support, U.S. Gov't, P.H.S. SAIDS Vaccines/ADMINISTRATION & DOSAGE/*IMMUNOLOGY SIV/GENETICS/*IMMUNOLOGY Vaccines, Attenuated/ADMINISTRATION & DOSAGE/*IMMUNOLOGYKWDjournalarticleaminoacidsequenceanimalantibodies,monoclonal/biosynthesis/KWDimmunologybasesequencebinding,competitiveblotting,westerncrossreactionsfluorescentantibodytechniquehumanhivenvelopeproteingp120/immunologyhiv-2/immunologyimmunoenzymetechniquesmacacamulatta/KWDimmunologymolecularsequencedataneutralizationtestspeptidemappingsupport,uKWDsKWDgov't,pKWDhKWDsKWDsaidsvaccines/administration&dosage/KWDimmunologysiv/genetics/KWDimmunologyvaccines,attenuated/administration&dosage/KWDimmunology
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Copyright © 1999 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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