دورية أكاديمية

CD8+ T Cell Activation Leads to Constitutive Formation of Liver Tissue-Resident Memory T Cells that Seed a Large and Flexible Niche in the Liver.

التفاصيل البيبلوغرافية
العنوان: CD8+ T Cell Activation Leads to Constitutive Formation of Liver Tissue-Resident Memory T Cells that Seed a Large and Flexible Niche in the Liver.
المؤلفون: Holz, Lauren E., Prier, Julia E., Freestone, David, Steiner, Thiago M., English, Kieran, Johnson, Darryl N., Mollard, Vanessa, Cozijnsen, Anton, Davey, Gayle M., Godfrey, Dale I., Yui, Katsuyuki, Mackay, Laura K., Lahoud, Mireille H., Caminschi, Irina, McFadden, Geoffrey I., Bertolino, Patrick, Fernandez-Ruiz, Daniel, Heath, William R.
المصدر: Cell Reports; Oct2018, Vol. 25 Issue 1, p68-68, 1p
مستخلص: Summary Liver tissue-resident memory T (Trm) cells migrate throughout the sinusoids and are capable of protecting against malaria sporozoite challenge. To gain an understanding of liver Trm cell development, we examined various conditions for their formation. Although liver Trm cells were found in naive mice, their presence was dictated by antigen specificity and required IL-15. Liver Trm cells also formed after adoptive transfer of in vitro -activated but not naive CD8+ T cells, indicating that activation was essential but that antigen presentation within the liver was not obligatory. These Trm cells patrolled the liver sinusoids with a half-life of 36 days and occupied a large niche that could be added to sequentially without effect on subsequent Trm cell cohorts. Together, our findings indicate that liver Trm cells form as a normal consequence of CD8+ T cell activation during essentially any infection but that inflammatory and antigenic signals preferentially tailor their development. Graphical Abstract Highlights • TCR stimulation is essential for liver Trm cell formation • Liver Trm cells require IL-15 • Local antigen presentation and inflammation enhance liver Trm cell formation • Newly formed liver Trm cells do not displace existing Trm cell populations Holz et al. demonstrate that tissue-resident memory T (Trm) cells routinely develop in the liver after T cell activation. Within the liver, IL-15, antigen, and inflammation aid Trm cell formation, but only IL-15 is essential. Newly formed Trm cells do not displace existing populations, demonstrating a flexible liver niche. [ABSTRACT FROM AUTHOR]
Copyright of Cell Reports is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:26391856
DOI:10.1016/j.celrep.2018.08.094