Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Maryam Yassai"'
Autor:
Sara E. Sabbagh, Dipica Haribhai, Jill A. Gershan, James Verbsky, James Nocton, Maryam Yassai, Elena N. Naumova, Erin Hammelev, Mahua Dasgupta, Ke Yan, Jack Gorski, Calvin B. Williams
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/1052c5151fa54bb9b97a939ee8a7ee29
Autor:
Sara E. Sabbagh, Dipica Haribhai, Jill A. Gershan, James Verbsky, James Nocton, Maryam Yassai, Elena N. Naumova, Erin Hammelev, Mahua Dasgupta, Ke Yan, Jack Gorski, Calvin B. Williams
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Recurrent exposures to a pathogenic antigen remodel the CD8+ T cell compartment and generate a functional memory repertoire that is polyclonal and complex. At the clonotype level, the response to the conserved influenza antigen, M158–66 has been we
Externí odkaz:
https://doaj.org/article/d54c6d29ecf14b399c9ea36992d8a7cf
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e43509 (2012)
Invariant natural killer T (iNKT) cells develop in the thymus and branch off from the maturation pathway of conventional T cell at the DP stage. While different stages of iNKT cellular development have been defined, the actual time that iNKT cell pre
Externí odkaz:
https://doaj.org/article/57a01d041a6f48a7865e7d8feb8adcf4
Publikováno v:
Molecular Immunology. 72:57-64
The amino acids at the V - J rearrangement junction of TCR are encoded by the D region, and by N or P nucleotides. Together they comprise the NDN region, the specific pMHC selection surface of the TCR β-chain. As an extension of our earlier work on
Publikováno v:
Human Immunology. 77:137-145
Generating a detailed description of human T cell repertoire diversity is an important goal in the study of human immunology. The circulation is the source of most T cells used for studies in humans. Here we use high throughput sequencing of TCR BV19
Autor:
Wendy Demos, D.V. Bosenko, Yashu Vashishath, Maryam Yassai, Vivian Zhou, Fong Lee, Jeyarani Regunathan, Jodie Box, Jack Gorski
Publikováno v:
Human Immunology. 74:809-817
The CD8 memory T cell repertoire to the influenza A derived M1(58-66) epitope shows a restricted V genes and CDR3 sequences usage. The repertoire is highly polyclonal and the clonotype distribution has been described as consisting of two components,
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 199(3)
The T cell repertoire is a function of thymic V(D)J rearrangement and of peripheral selection. The mature repertoire embodies TCR sequences that are important for survival and can identify important structural aspects of the TCR. Analysis of the circ
Publikováno v:
Transfusion. 57:1092-1093
Autor:
A. W. Chen, Petra Wise, Erica G. Schmitt, Nita H. Salzman, Talal A. Chatila, Calvin B. Williams, Brandon Edwards, Jennifer Ziegelbauer, Pippa Simpson, Shuang Jia, Lance M. Relland, Maryam Yassai, Derek W. Nickerson, Yu Qian Zheng, Shun Hwa Li, Martin J. Hessner, Jack Gorski, Jason B. Williams, Dipica Haribhai
Publikováno v:
Immunity. 35:109-122
SummaryAlthough both natural and induced regulatory T (nTreg and iTreg) cells can enforce tolerance, the mechanisms underlying their synergistic actions have not been established. We examined the functions of nTreg and iTreg cells by adoptive transfe
Publikováno v:
The Journal of Immunology. 186:6617-6624
The aging of T cell memory is often considered in terms of senescence, a process viewed as decay and loss of memory T cells. How senescence would affect memory is a function of the initial structure of the memory repertoire and whether the clonotypes