
Science Immunology
- Volume 7
- Issue 77
- Nov 2022

ONLINE COVER Rejuvenation Potential of TRM Subsets. This month’s cover depicts a “fountain of youth” from which new tissue resident memory T cells (TRM) are emerging after a secondary infectious challenge. Newly formed CD103– TRM (blue) and CD103+ TRM (red) are derived from proliferating, CD103– precursor cells and join the pool of preexisting CD103+ TRM (gray) that lack this restorative capacity. This model for TRM replenishment is supported by new fate-mapping mouse models described in separate papers by von Hoesslin and Kuhlmann et al. and Fung et al. that are discussed in a Focus by Jensen and Farber.
Credit: Ella Maru Studio- Alejandro V. Villarino
- Arian DJ Laurence
- et al.
A central role for STAT5 in the transcriptional programing of T helper cell metabolism
- Hanna S. Hong
- Nneka E. Mbah
- et al.
OXPHOS promotes apoptotic resistance and cellular persistence in TH17 cells in the periphery and tumor microenvironment
- Leslie Naesens
- Santoshi Muppala
- et al.
GTF3A mutations predispose to herpes simplex encephalitis by disrupting biogenesis of the host-derived RIG-I ligand RNA5SP141
- Alexander Muik
- Bonny Gaby Lui
- et al.
Omicron BA.2 breakthrough infection enhances cross-neutralization of BA.2.12.1 and BA.4/BA.5
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Science Immunology publishes original, peer-reviewed, science-based research articles that report critical advances in all areas of immunological research, including important new tools and techniques.
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