TY - JOUR
T1 - Characterization of a polyclonal cytolytic T lymphocyte response to human immunodeficiency virus in persons without clinical progression
AU - Lubaki, N. M.
AU - Ray, S. C.
AU - Dhruva, B.
AU - Quinn, T. C.
AU - Siliciano, R. F.
AU - Bollinger, R. C.
PY - 1997
Y1 - 1997
N2 - A total of 82 human immunodeficiency virus (HIV)-l-specific cytolytic T lymphocyte (CTL) clones were isolated and characterized from 5 HIV-infected subjects, utilizing multiple HLA class I alleles. B62-restricted. HIV-1 gag- specific CTL clones isolated from a single blood sample from I subject used four different Vβ gene rearrangements. Multiple CTL clones could be isolated from the same time point directed against HIV-1 gag, nef, and env from 1 subject. A prospective analysis resulted in the isolation of CTL clones from 1 subject directed against multiple HIV-1 antigens, including the same highly conserved nef peptide, over a 1-year period, in the absence of detectable circulating viral plasma RNA. These data suggest that in some persons without clinical progression and low levels of circulating HIV-1, the CTL response is polyclonal, is directed against multiple HIV-1 proteins, including highly conserved peptides within these proteins, and is maintained over time.
AB - A total of 82 human immunodeficiency virus (HIV)-l-specific cytolytic T lymphocyte (CTL) clones were isolated and characterized from 5 HIV-infected subjects, utilizing multiple HLA class I alleles. B62-restricted. HIV-1 gag- specific CTL clones isolated from a single blood sample from I subject used four different Vβ gene rearrangements. Multiple CTL clones could be isolated from the same time point directed against HIV-1 gag, nef, and env from 1 subject. A prospective analysis resulted in the isolation of CTL clones from 1 subject directed against multiple HIV-1 antigens, including the same highly conserved nef peptide, over a 1-year period, in the absence of detectable circulating viral plasma RNA. These data suggest that in some persons without clinical progression and low levels of circulating HIV-1, the CTL response is polyclonal, is directed against multiple HIV-1 proteins, including highly conserved peptides within these proteins, and is maintained over time.
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U2 - 10.1086/516468
DO - 10.1086/516468
M3 - Article
C2 - 9180175
AN - SCOPUS:0030918617
SN - 0022-1899
VL - 175
SP - 1360
EP - 1367
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 6
ER -