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Michèl R. Klein

Researcher at Leiden University Medical Center

Publications -  113
Citations -  9069

Michèl R. Klein is an academic researcher from Leiden University Medical Center. The author has contributed to research in topics: Cytotoxic T cell & Antigen. The author has an hindex of 51, co-authored 113 publications receiving 8801 citations. Previous affiliations of Michèl R. Klein include Medical Research Council & University of Amsterdam.

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Phenotypic and Functional Separation of Memory and Effector Human CD8+ T Cells

TL;DR: In this article, two discrete primed subpopulations are found within the circulating human CD8+ T cell subset, i.e., CD45RA−CD45R0+ cells and CD27−CD27− cells.
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Kinetics of Gag-specific cytotoxic T lymphocyte responses during the clinical course of HIV-1 infection: a longitudinal analysis of rapid progressors and long-term asymptomatics.

TL;DR: In the long-term asymptomatics, persistent HIV-1 Gag-specific CTL responses and very low numbers of HIV- 1-infectedCD4+ T cells coincided with normal and stable CD4+ counts and preserved CD3 mAb-induced T cell reactivity for more than 8 yr.
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Mass accumulation rates in asia during the cenozoic

TL;DR: In this article, the authors established estimates of mass accumulation rates in 18 mostly offshore sedimentary basins in Asia since the beginning of the Cenozoic, ≈ 66.
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Human T-cell responses to 25 novel antigens encoded by genes of the dormancy regulon of Mycobacterium tuberculosis.

TL;DR: Especially strong IFN-gamma responses to latency antigens were observed in latently infected individuals, suggesting that immune responses against these antIGens may contribute to controlling latent M. tuberculosis infection.
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Human immunodeficiency virus type 1 Rev- and Tat-specific cytotoxic T lymphocyte frequencies inversely correlate with rapid progression to AIDS

TL;DR: It is shown in twelve HIV-1-infected individuals that detection of Rev-specific CTL precursors (CTLp) early in the asymptomatic stage, as well as detection ofRev- and Tat- specific CTLp later during follow-up, inversely correlate with rapid disease progression, in agreement with the hypothesis that CTL against proteins that are important for early viral transcription and translation are of particular importance in protection from rapid Disease progression.