Table 1.
Markers | Alternative name(s) | Marker location | Expression on resting Treg | Expression level upon activation |
---|---|---|---|---|
CD25 | IL-2Rα | Surface | CD25high | Very high |
FOXP3 | N/A | Intranuclear | FOXP3high | Very high |
CD127 | IL-7Rα | Surface | CD127low/- | Low/- |
CD45RA | N/A | Surface | Naïve Treg are predominantly CD45RA+ | Low/- |
CD45RO | N/A | Surface | Memory Treg are predominantly CD45RO+ | High |
CD62L | L-selectin | Surface | Treg with secondary lymph node homing capacity are predominantly CD62L+ | Retained |
CCR7 | CD197 | Surface | Most of the Treg with secondary lymph node homing capacity are CCR7+ | Retained |
CD95 | Fas | Surface | Most of the naïve Treg are CD95low/- | High |
CD44 | N/A | Surface | Most of the Treg are CD44low/- | High |
CD31 | PECAM-1 | Surface | Recent thymic emigrant Treg are CD31+ | Low |
Helios | IKZF2 | Intranuclear | Thymus derived stable Treg are Helios+ | Stable over time |
GPA33 | A33 | Surface | Pure and stable naïve Treg population, that are also derived from thymus, are GPA33+ | low |
CTLA-4 | CD152 | Surface/Intracellular | Treg express CTLA-4 constitutively at low level | High |
PD-1 | CD279 | Surface/Intracellular | Most of the PD-1 expressing Treg retain its expression in the intracellular compartments | High (surface) |
ICOS | CD278 | Surface | About 20% of the peripheral Treg are ICOS+ | High |
TIGIT | VSTM3 | Surface | Few Treg with activated phenotype are TIGIT+ | High |
LAG-3 | CD223 | Surface | Most of the resting Treg are LAG3low/- | High |
TIM-3 | CD366 HAVCR2 |
Surface | Only 2-5% of Treg in periphery are TIM-3+ | High |
GITR | TNFRSF18 CD357 |
Surface | Few Treg with activated phenotype are GITR+ | High |
OX-40 | CD134 | Surface | Few Treg with activated phenotype are OX-40+ | High |
4-1BB | CD137 | Surface | Few Treg with activated phenotype are 4-1BB+ | High |
CD27 | N/A | Surface | Treg with high suppressive capacity are CD27+ | Mostly stable over time |
CD49d | α4 integrin VLA-4 α | Surface | 70% of the immunosuppressive FOXP3+ Treg are CD49dlow/- | High |
CD26 | ADA binding protein | Surface | Most of the Treg are CD26low/- | High |
CD6 | – | Surface | Most of the Treg are CD6low/- | High |
CD226 | DNAM-1 | Surface | Most of the Treg are CD226low/- | High |
TGF-b | TGF-b1, LAP | Surface/Intracellular | Most of the resting Treg are TGF-blow/- | High |
LAP | TGF-b1 | Surface/Intracellular | Most of the resting Treg are LAPlow/- | High |
GARP | LRRC32 | Surface | Most of the resting Treg are GARPlow/- | High |
CD39 | N/A | Surface | Only effector/memory-like Treg are CD39+ | High |
CD73 | N/A | Surface/Intracellular | Most of the CD73 expressing Treg retain in the intracellular compartments | High (surface) |
CD121a/b | IL-1R I/II | Surface | Most of the resting Treg are CD121a/blow/- | High (transient) |
CD69 | N/A | Surface | Most of the resting Treg are CD69low/- | High |
HLA-DR | N/A | Surface | Few Treg with activated phenotype are HLA-DR+ | High |
CD101 | BB27 | Surface | Less studied in humans | N/A |
CD129 | IL-9R | Surface | Less studied in humans | N/A |
CD103 | Integrin αEβ7 | Surface | <5% Treg in various tissues, including blood are CD103+ | N/A |
Neuropilin-1 | CD304 | Surface | Thymic derived mouse Treg are Neuropilin-1+ (Human studies are controversial) | N/A |
CD70 | CD27L | Surface | Only 5-6% Tregs are CD70+ | High |
CD80/CD86 | B7 1/2 | Surface | 20% Treg are CD80+ and <1% Treg are CD86+ | High |
References are indicated in the text.
The table above presents an overview of human Treg markers that delineate different subsets of Treg cells, along with their respective properties, as detailed in the review.