Publication | Closed Access
A Subset of CD4 <sup>+</sup> Thymocytes Selected by MHC Class I Molecules
456
Citations
52
References
1994
Year
Most ImmatureMhc ClassLymphocyte DevelopmentAdaptive Immune SystemT-regulatory CellImmunologyImmune RegulationCd4 T Cell ResponsesImmune SystemImmunotherapyImmunogeneticsSimultaneous EngagementAlpha Beta TcrsCell SignalingAutoimmune DiseaseAllergyAutoimmunityT Cell ImmunityCell BiologyImmune Cell DevelopmentCellular Immune ResponseMedicine
To complete their maturation, most immature thymocytes depend on the simultaneous engagement of their antigen receptor [alpha beta T cell receptor (TCR)] and their CD4 or CD8 coreceptors with major histocompatibility complex class II or I ligands, respectively. However, a normal subset of mature alpha beta TCR+ thymocytes did not follow these rules. These thymocytes expressed NK1.1 and a restricted set of alpha beta TCRs that are intrinsically class I-reactive because their positive selection was class I-dependent but CD8-independent. These cells were CD4+ and CD4-8- but never CD8+, because the presence of CD8 caused negative selection. Thus, neither CD4 nor CD8 contributes signals that direct their maturation into the CD4+ and CD4-8- lineages.
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