CD28


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CD28

a type I transmembrane protein present on most CD4 T cells, many CD8 T cells, and most plasma cells that enhances the transcription and stability of IL-2 messenger RNA.
References in periodicals archive ?
AB103 is a rationally designed short peptide that modulates the patient's inflammatory response through binding to the CD28 dimer interface.
Transcription analysis of 44 CD genes was also carried out, indicating 24 CD genes (CD3E, CD244, CD69, CD247, CD40L, CD38, CD5L, CD44, CD5, CD83, CD163L1, CD36, CD14, CD28, CD200R1A, CD40, CD59, CD200, CD4, CD2, CD72, CD180, CD79B, and CD93) to be markedly increased by 2.
CD3, CD4, CD9, CD11, CD19, CD20, CD22, CD26, CD27, CD28, CD29, CD33, CD37, CD40, CD44, CD45, CD47, CD52u CD55, CD56, CD66, CD70, CD74, CD80, CD95, CD98, CD100, CD117, CD135, CD137, CD152, CD200, CD223, CD227, CD246, CD248, CD274, CD276, CD279
Differences in allergen-induced T cell activation between allergic asthma and rhinitis: Role of CD28, ICOS and CTLA-4.
Afterwards, cells were stimulated with antihuman CD3 (clone OKT3) and anti-human CD28 (clone 28.
CD28 loss in senescent CD4+ T-cells: reversal by interleukin-12 stimulation.
Human neutrophil-expressed CD28 interacts with mscrophage B7 to induce phosphatidylinosito 13-kinase-dependent IFN- secretion and restriction of Leishmania growth.
Gila Arad and licensed from Yissum, the technology transfer company of the Hebrew University, is a rationally designed, short peptide that modulates the host's inflammatory response through binding to the CD28 dimer interface.
Also important are LFA-1, ICAM-1, CD28, and CD80/CD86.
One-unit increases in the expression of 7 of the 36 genes evaluated (PDCD11, LATS2, TRIM13, CD28, SMC1A, IL7R, and NIPBL) were associated with significantly lower MNBN frequencies, with MR ranging from 0.
CD28 is another immune checkpoint molecule on T cells responsible for the activation of resting T cells; therefore, it is dubbed the "accelerator pedal" of T cells.
They down-regulate the level of expression of major histo-compatibility complex (MHC) class II molecules as well as the cluster of differentiation (CD) 20 and CD28 co-stimulatory molecules on antigen-presenting cells (APCs).