Immunization with human immunodeficiency virus type 1 rgp120W61D in QS21/MPL adjuvant primes T cell proliferation and C-C chemokine production to multiple epitopes within variable and conserved domains of gp120W61D. 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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Immunization with human immunodeficiency virus type 1 rgp120W61D in QS21/MPL adjuvant primes T cell proliferation and C-C chemokine production to multiple epitopes within variable and conserved domains of gp120W61D.

J Infect Dis. 1999 Mar;179(3):558-66. Unique Identifier : AIDSLINE MED/99137790
Jones GJ; von Hoegen P; Weber J; Rees AD; GU Medicine and Communicable Diseases, Imperial College School of; Medicine at St. Mary's, London, W2 1PG, United Kingdom.; gareth.jones@ic.ac.uk


Abstract: Human immunodeficiency virus type 1 (HIV-1) gp120W61D-specific T cell lines (TCL) were generated from an HIV-1-seronegative volunteer who received rgp120W61D in QS21/MPL adjuvant with emulsion. TCL were challenged with pools of consecutive, overlapping peptides spanning the gp120W61D sequence and then with the individual peptides of the immunostimulatory pool. T cell epitopes were found within both variable and conserved domains, and there was no evidence of a single immunodominant epitope. The two most frequently recognized peptides were located in the C1 domain and in the C-terminal region of the V3 loop. Several TCL were shown to recognize multiple peptides from nonoverlapping regions. Peptides from both conserved and variable domains were capable of inducing MIP-1alpha, MIP-1beta, and RANTES production. When tested against the equivalent peptide from the HIV-1IIIB sequence, however, TCL were able to tolerate only minor conserved changes in the amino acid sequence.
Keywords: JOURNAL ARTICLE Amino Acid Sequence Amino Acid Substitution *AIDS Vaccines Cell Line Chemokines, CC/*BIOSYNTHESIS/GENETICS Conserved Sequence CD4-Positive T-Lymphocytes Epitopes/CHEMISTRY/IMMUNOLOGY Human HIV Envelope Protein gp120/CHEMISTRY/GENETICS/*IMMUNOLOGY HIV-1/*IMMUNOLOGY *Lymphocyte Transformation Molecular Sequence Data Mutagenesis, Site-Directed Protein Structure, Secondary Recombinant Proteins/CHEMISTRY/IMMUNOLOGY Support, Non-U.S. Gov't T-Lymphocytes/*IMMUNOLOGY *Vaccines, SyntheticKWDjournalarticleaminoacidsequenceaminoacidsubstitutionKWDaidsvaccinescelllinechemokines,cc/KWDbiosynthesis/geneticsconservedsequencecd4-positivet-lymphocytesepitopes/chemistry/immunologyhumanhivenvelopeproteingp120/chemistry/genetics/KWDimmunologyhiv-1/KWDimmunologyKWDlymphocytetransformationmolecularsequencedatamutagenesis,site-directedproteinstructure,secondaryrecombinantproteins/chemistry/immunologysupport,non-uKWDsKWDgov'tt-lymphocytes/KWDimmunologyKWDvaccines,synthetic
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