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Research Article Free access | 10.1172/JCI117851

Immune predispositions for cytomegalovirus retinitis in AIDS. The HNRC Group.

R D Schrier, W R Freeman, C A Wiley, and J A McCutchan

Department of Pathology, University of California, San Diego, La Jolla 92093, USA.

Find articles by Schrier, R. in: PubMed | Google Scholar

Department of Pathology, University of California, San Diego, La Jolla 92093, USA.

Find articles by Freeman, W. in: PubMed | Google Scholar

Department of Pathology, University of California, San Diego, La Jolla 92093, USA.

Find articles by Wiley, C. in: PubMed | Google Scholar

Department of Pathology, University of California, San Diego, La Jolla 92093, USA.

Find articles by McCutchan, J. in: PubMed | Google Scholar

Published April 1, 1995 - More info

Published in Volume 95, Issue 4 on April 1, 1995
J Clin Invest. 1995;95(4):1741–1746. https://doi.org/10.1172/JCI117851.
© 1995 The American Society for Clinical Investigation
Published April 1, 1995 - Version history
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Abstract

CMV retinitis develops in approximately 28-35% of all AIDS patients at later stages of disease, often leading to blindness. To determine whether the subset of AIDS patients who developed CMV retinitis (CMV-R) were immunologically predisposed, T cell proliferation responses to CMV were examined prospectively in an HIV infected, HLA typed, longitudinal study population. Individuals who developed CMV-R had significantly lower T cell proliferation responses to CMV, both early and late in disease, compared to CD4 matched controls who have not developed CMV-R. Since HLA proteins influence T-cell recognition, phenotypes of 21 CMV-R patients were examined to determine whether certain HLA alleles were associated with low immune response and predisposed AIDS patients to CMV-R. HLA DR7 and B44 were at increased (nearly twice the expected) frequency in those with CMV-R. The combined association of either B44, 51 or DR7 with CMV-R was highly significant (P = .008, relative risk of CMV-R = 15) with correction for multiple comparisons. Low immune responses were twice as frequent in those with (61%) compared to those without (30%) predisposing alleles. Thus, AIDS patients with immunogenetically related hyporesponsiveness to CMV antigens may be at increased risk of retinitis.

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