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. 2022 Aug 29;52(10):1547–1560. doi: 10.1002/eji.202149759

Table 1.

Markers of tissue‐resident memory T cells

Marker Up/down Function Site Notes Mouse Reference Human Reference
CCR9 migration SI>LI [18]
α4β7 migration SI, LI? early upregulation, decreased in memory phase [levels that from 21, 22]
CXCR3 migration SI? LI [24]
CD103

binds to

E‐cadherin

SI, LI necessary for cell accumulation but not retention [22] [25]
CD69 inhibits S1pr1 SI, LI dispensable for Trm retention in mouse intestine [26] [25]
CD49a

binds

to collagen IV

skin not studied in intestine [27] [28]
S1pr1 cell egress SI, LI? regulated by KLF2 [29]
S1pr5 cell egress skin not studied in intestine [30]
CCR7 LN homing skin not studied in intestine [31]

Transcription

factors

Hobit inhibits cell egress SI, LI? in humans, it can be expressed by circulating memory cells and liver resident NK cells [32] [33, 34]
Blimp1 inhibits cell egress SI, LI? early upregulation, lower level in Trm [32]
Runx3 promotes residency SI, LI? [35]
Bhlhe40 promotes Trm mitochondrial fitness and epigenetic programming Lung and tumor [36]
Junb/Fosl2 not well studied SI, LI? [37]
Klf2 promotes cell egress SI, LI? [29]