# Cytotoxic CD4+ T cells: origin, biological functions, diseases and therapeutic targets

**Authors:** Longyong Lai, Shuan Ran, Yuan Li, Jikai Cui, Xi Zhang, Jizhang Yu, Yanqiang Zou, Cheng Zhou, Jiahong Xia, Jie Wu

PMC · DOI: 10.1038/s41392-025-02533-z · Signal Transduction and Targeted Therapy · 2026-03-09

## TL;DR

This review explores cytotoxic CD4+ T cells, their unique functions in immune responses, roles in various diseases, and potential as therapeutic targets.

## Contribution

The paper provides a comprehensive synthesis of recent findings on cytotoxic CD4+ T cells, emphasizing their roles in disease and therapeutic potential.

## Key findings

- Cytotoxic CD4+ T cells exhibit cytotoxicity similar to CD8+ T cells, showing functional plasticity.
- These cells contribute to disease progression in cancer, infections, autoimmunity, and cardiovascular conditions.
- The paper summarizes therapeutic strategies targeting cytotoxic CD4+ T cells and clinical trial data.

## Abstract

Cytotoxic CD4+ T lymphocytes are a unique subset of CD4+ T cells characterized by their cytokine secretion and cytolytic activity. Unlike traditional CD4+ helper T cells, cytotoxic CD4+ T lymphocytes exhibit similar cytotoxicity to that of CD8+ T cells, revealing unexpected plasticity in CD4+ T-cell functions. This flexibility suggests that CD4+ T cells can transform and acquire effector functions beyond their conventional functions, emphasizing their importance in various immune responses. Despite the identification of cytotoxic CD4+ T lymphocytes decades ago, recent advancements have broadened our understanding of their phenotypic diversity, transcriptional regulation, differentiation pathways, and functional roles. Cytotoxic CD4+ T lymphocytes play pivotal roles across a broad spectrum of diseases, including cancer, infectious diseases, autoimmune disorders, and cardiovascular diseases. They typically mediate strong inflammatory responses and kill target cells through cytotoxicity, playing a crucial role in maintaining immune homeostasis. In this review, we synthesize current findings on cytotoxic CD4+ T lymphocytes, emphasizing their origin, biomarkers, regulatory molecules, and biological functions. Additionally, we focus on their pathological roles in the progression of various diseases and examine how cytotoxic CD4+ T lymphocytes contribute to disease development and progression. We also provide a comprehensive summary of therapeutic strategies targeting cytotoxic CD4+ T cells and review the associated clinical trial data, aiming to propose new strategies for disease management through the targeting of cytotoxic CD4+ T lymphocytes.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** CASP9 (caspase 9) [NCBI Gene 842] {aka APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56}, SLAMF7 (SLAM family member 7) [NCBI Gene 57823] {aka 19A, CD319, CRACC, CS1}, HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, Stat5a (signal transducer and activator of transcription 5A) [NCBI Gene 20850] {aka STAT5}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, CD27 (CD27 molecule) [NCBI Gene 939] {aka S152, S152. LPFS2, T14, TNFRSF7, Tp55}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, HLA-G (major histocompatibility complex, class I, G) [NCBI Gene 3135] {aka MHC-G}, IL7 (interleukin 7) [NCBI Gene 3574] {aka IL-7, IMD130}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, TNFRSF1B (TNF receptor superfamily member 1B) [NCBI Gene 7133] {aka CD120b, TBPII, TNF-R-II, TNF-R75, TNFBR, TNFR1B}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, KIR2DL4 (killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4) [NCBI Gene 3805] {aka CD158D, G9P, KIR-103AS, KIR-2DL4, KIR103, KIR103AS}, CLEC4D (C-type lectin domain family 4 member D) [NCBI Gene 338339] {aka CD368, CLEC-6, CLEC6, CLECSF8, Dectin-3, MCL}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, CYCS (cytochrome c, somatic) [NCBI Gene 54205] {aka CYC, HCS, THC4}, TNFRSF9 (TNF receptor superfamily member 9) [NCBI Gene 3604] {aka 4-1BB, CD137, CDw137, ILA, IMD109}, KLRC1 (killer cell lectin like receptor C1) [NCBI Gene 3821] {aka CD159A, NKG2, NKG2A}, Zeb2 (zinc finger E-box binding homeobox 2) [NCBI Gene 24136] {aka 9130203F04Rik, D130016B08Rik, SIP1, Zfhx1b, Zfx1b, Zfxh1b}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, Slc7a5 (solute carrier family 7 (cationic amino acid transporter, y+ system), member 5) [NCBI Gene 20539] {aka 4F2LC, D0H16S474E, Gm42049, LAT1, TA1}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, CD80 (CD80 molecule) [NCBI Gene 941] {aka B7, B7-1, B7.1, BB1, CD28LG, CD28LG1}, SELL (selectin L) [NCBI Gene 6402] {aka CD62L, LAM1, LECAM1, LEU8, LNHR, LSEL}, ZNF683 (zinc finger protein 683) [NCBI Gene 257101] {aka Hobit}, KAR [NCBI Gene 8083], XCL2 (X-C motif chemokine ligand 2) [NCBI Gene 6846] {aka SCM-1b, SCM1B, SCYC2}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, TNFRSF10B (TNF receptor superfamily member 10b) [NCBI Gene 8795] {aka CD262, DR5, KILLER, KILLER/DR5, TRAIL-R2, TRAILR2}, KCNN4 (potassium calcium-activated channel subfamily N member 4) [NCBI Gene 3783] {aka DHS2, IK, IK1, IKCA1, KCA4, KCa3.1}, TLR9 (toll like receptor 9) [NCBI Gene 54106] {aka CD289}, ITGAM (integrin subunit alpha M) [NCBI Gene 3684] {aka CD11B, CR3A, HNA-4, MAC-1, MAC1A, MO1A}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, CXADRP1 (CXADR pseudogene 1) [NCBI Gene 653108] {aka CAR, CXADRP}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, OGA (O-GlcNAcase) [NCBI Gene 10724] {aka MEA5, MGEA5, NCOAT}, CXCL9 (C-X-C motif chemokine ligand 9) [NCBI Gene 4283] {aka CMK, Humig, MIG, SCYB9, crg-10}, IFNB1 (interferon beta 1) [NCBI Gene 3456] {aka IFB, IFF, IFN-beta, IFNB}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, GZMB (granzyme B) [NCBI Gene 3002] {aka C11, CCPI, CGL-1, CGL1, CSP-B, CSPB}, LILRB1 (leukocyte immunoglobulin like receptor B1) [NCBI Gene 10859] {aka CD85J, ILT-2, ILT2, LIR-1, LIR1, MIR-7}, IL27RA (interleukin 27 receptor subunit alpha) [NCBI Gene 9466] {aka CRL1, IL-27RA, IL27R, TCCR, WSX1, zcytor1}, Pik3r1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 18708] {aka PI3K, p50alpha, p55alpha, p85alpha}, PRDM1 (PR/SET domain 1) [NCBI Gene 639] {aka BLIMP-1, BLIMP1, PRDI-BF1}, CCL4 (C-C motif chemokine ligand 4) [NCBI Gene 6351] {aka ACT2, AT744.1, G-26, HC21, LAG-1, LAG1}, TRDC (T cell receptor delta constant) [NCBI Gene 28526] {aka TCRD}, IL7R (interleukin 7 receptor) [NCBI Gene 3575] {aka CD127, CDW127, IL-7R-alpha, IL-7Ralpha, IL7RA, IL7Ralpha}, Runx3 (runt related transcription factor 3) [NCBI Gene 12399] {aka AML2, Cbfa3, Pebp2a3, Rx3}, Il2 (interleukin 2) [NCBI Gene 16183] {aka Il-2}, Hdac1 (histone deacetylase 1) [NCBI Gene 433759] {aka HD1, Hdac1-ps, MommeD5, RPD3}, KCNA3 (potassium voltage-gated channel subfamily A member 3) [NCBI Gene 3738] {aka HGK5, HLK3, HPCN3, HUKIII, KV1.3, MK3}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, BCL2L11 (BCL2 like 11) [NCBI Gene 10018] {aka BAM, BIM, BOD}
- **Diseases:** arrhythmia (MESH:D001145), multiorgan dysfunction (MESH:D009102), Autoimmune diseases (MESH:D001327), CHF (MESH:D006333), B-ALL (MESH:D015452), breast cancer (MESH:D001943), obesity (MESH:D009765), lung allograft dysfunction (MESH:D000092122), IBD (MESH:D015212), CMV (MESH:D003586), inflammatory cytokines (MESH:D000080424), peripheral embolism (MESH:D004617), type 2 diabetes (MESH:D003924), lymphoma (MESH:D008223), thymic leukemia (MESH:D013953), CAD (MESH:D003324), stroke (MESH:D020521), muscle pain (MESH:D063806), sudden cardiac death (MESH:D016757), liver injury (MESH:D017093), cardiac allograft vasculopathy (MESH:D006331), pathological damage (MESH:D005598), hepatitis (MESH:D056486), functional disability (MESH:D003291), myocardial injury (MESH:D009202), Hodgkin lymphoma (MESH:D006689), viremia (MESH:D014766), chronic hepatitis B (MESH:D019694), blood cancers (MESH:D019337), acute respiratory distress syndrome (MESH:D012128), fever (MESH:D005334), necrosis (MESH:D009336), intestinal damage (MESH:D007410), acute myeloid leukemia (MESH:D015470), atherosclerotic plaques (MESH:D058226), immune dysregulation (OMIM:614878), diffuse large B-cell lymphoma (MESH:D016403), HIV (MESH:D015658), metabolic disorders (MESH:D008659), HCC (MESH:D006528), Infectious diseases (MESH:D003141), cognitive impairment (MESH:D003072), unstable angina (MESH:D000789), head and neck squamous cell carcinoma (MESH:D000077195), glioblastoma (MESH:D005909), bladder cancer (MESH:D001749), autoimmune hepatitis (MESH:D019693), non-small cell lung cancer (MESH:D002289), SLE systemic lupus erythematosus (MESH:D008180), UC (MESH:D003093), myocardial or vascular tissue damage (MESH:D017695), EBV-related diseases (MESH:D020031), RA (MESH:D001172), Fibrosis (MESH:D005355), melanoma (MESH:D008545), acute-on-chronic liver failure (MESH:D065290), injury (MESH:D014947), pancreatic ductal adenocarcinoma (MESH:D021441), medium- and large-vessel vasculitis (MESH:D014657), T-cell dysfunction (MESH:C536780)
- **Chemicals:** luminal (MESH:D010634), vitamin A (MESH:D014801), lipid (MESH:D008055), tryptophan (MESH:D014364), maraviroc (MESH:D000077592), infliximab (MESH:D000069285), calcium (MESH:D002118), ceramide (MESH:D002518), reactive oxygen species (MESH:D017382), nitric oxide (MESH:D009569), indole (MESH:C030374), vitamin D (MESH:D014807), mycophenolate mofetil (MESH:D009173), LEX (-), everolimus (MESH:D000068338), oxygen (MESH:D010100), ustekinumab (MESH:D000069549), Retinoic acid (MESH:D014212), tacrolimus (MESH:D016559), NADPH (MESH:D009249), poly(I:C) (MESH:D011070), nilotinib (MESH:C498826)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Human immunodeficiency virus 1 (no rank) [taxon 11676], Human alphaherpesvirus 3 (Varicella-zoster virus, no rank) [taxon 10335], Limosilactobacillus reuteri (species) [taxon 1598], Human immunodeficiency virus (species) [taxon 12721], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mus musculus (house mouse, species) [taxon 10090], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Faecalibacterium prausnitzii (species) [taxon 853], Homo sapiens (human, species) [taxon 9606], Clostridium (genus) [taxon 1485]
- **Mutations:** rs7574865

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12972364/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12972364/full.md

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Source: https://tomesphere.com/paper/PMC12972364