Michael A. EllerNilu GoonetillekeBoonrat TassaneetrithepLeigh Anne EllerMargaret C. CostanzoSusan JohnsonMichael R. BettsShelly J. KrebsBonnie M. SlikeSorachai NitayaphanKathleen RonoSodsai TovanabutraLucas MagangaHannah KibuukaLinda JagodzinskiSheila PeelMorgane RollandMary A. MarovichJerome H. KimNelson L. MichaelMerlin L. RobbHendrik StreeckWalter Reed Army Institute of ResearchHJFThe University of North Carolina at Chapel HillMahidol UniversityUniversity of PennsylvaniaArmed Forces Research Institute of Medical Sciences, ThailandWalter Reed Project-KenyaWalter Reed Program-TanzaniaMakerere UniversityUniversitats Klinikum Essen und Medizinische FakultatInternational Vaccine Institute, SeoulNational Institute of Allergy and Infectious Diseases2018-12-112019-03-142018-12-112019-03-142016-04-01Journal of Virology. Vol.90, No.8 (2016), 4005-4016109855140022538X2-s2.0-84963864427https://repository.li.mahidol.ac.th/handle/20.500.14594/41314© 2016, American Society for Microbiology. Attrition within the CD4+T cell compartment, high viremia, and a cytokine storm characterize the early days after HIV infection. When the first emerging HIV-specific CD8+T cell responses gain control over viral replication it is incomplete, and clearance of HIV infection is not achieved even in the rare cases of individuals who spontaneously control viral replication to nearly immeasurably low levels. Thus, despite their partial ability to control viremia, HIV-specific CD8+T cell responses are insufficient to clear HIV infection. Studying individuals in the first few days of acute HIV infection, we detected the emergence of a unique population of CD38+CD27-CD8+T cells characterized by the low expression of the CD8 receptor (CD8dim). Interestingly, while high frequencies of HIV-specific CD8+T cell responses occur within the CD38+CD27-CD8dimT cell population, the minority populations of CD8brightT cells are significantly more effective in inhibiting HIV replication. Furthermore, the frequency of CD8dimT cells directly correlates with viral load and clinical predictors of more rapid disease progression. We found that a canonical burst of proliferative cytokines coincides with the emergence of CD8dimT cells, and the size of this population inversely correlates with the acute loss of CD4+T cells. These data indicate, for the first time, that early CD4+T cell loss coincides with the expansion of a functionally impaired HIV-specific CD8dimT cell population less efficient in controlling HIV viremia.Mahidol UniversityAgricultural and Biological SciencesImmunology and MicrobiologyArticleSCOPUS10.1128/JVI.02785-15