# Distribution and clinical significance of peripheral blood lymphocyte PD-1 and PD-L1 in non-Hodgkin lymphoma: a retrospective study in Chinese patients

**Authors:** Lu Liu, Lei Wang, Wei Wang, Yansu Wang, Yanrong Wang, Na Xu, Na Li, Haifeng Liu

PMC · DOI: 10.3389/fonc.2026.1683486 · Frontiers in Oncology · 2026-02-12

## TL;DR

This study shows that PD-1 and PD-L1 levels in blood lymphocytes are linked to disease severity and treatment outcomes in non-Hodgkin lymphoma patients.

## Contribution

The study provides new insights into the clinical relevance of PD-1 and PD-L1 in peripheral blood lymphocytes for non-Hodgkin lymphoma in a Chinese population.

## Key findings

- Higher PD-1 and PD-L1 levels on CD8+ T cells were found in patients with elevated LDH.
- PD-1 on CD8+ T cells was higher in patients with bone marrow involvement.
- Lower PD-L1 levels on T cells were associated with better treatment response.

## Abstract

Programmed death-1 (PD-1) and its ligand PD-L1 play critical roles in immune checkpoint regulation. This study investigated the relationship between PD-1 and PD-L1 expression on peripheral blood lymphocytes and Non- Hodgkin Lymphoma progression.

This retrospective study included patients diagnosed with Non- Hodgkin Lymphoma at Jilin Cancer Hospital between October 2013 and May 2017. PD-1 and PD-L1 expression on CD4+ and CD8+ T cells was analyzed using flow cytometry.

A total of 125 non- Hodgkin Lymphoma patients (65 males and 60 females; median age, 57 years; range, 14–86 years) were included. PD-1 and PD-L1 expression on CD8+ T cells was significantly higher in patients with elevated lactate dehydrogenase (LDH) (>245 U/L) than in those with normal LDH (PD-1: 16.46% vs. 12.68%, P = 0.005; PD-L1: 9.96% vs. 7.90%, P = 0.043). PD-1 expression on CD8+ T cells was also higher in patients with bone marrow involvement compared with those without (17.62% vs. 14.56%, P = 0.039). Furthermore, PD-L1 expression on both CD4+ and CD8+ T cells was significantly lower in patients who achieved complete response (CR) compared with those with non-CR (CD4+: 11.14% vs. 18.61%, P<0.001; CD8+: 7.19% vs. 10.60%, P = 0.032). Notably, a decrease in CD4+ PD-1 levels after treatment showed a strong trend towards improved overall survival compared with cases showing increased levels (median survival not reached in the decreased group vs. 41.77 months in the increased group, P = 0.066).

Peripheral blood lymphocyte PD-1 and PD-L1 expression are associated with LDH levels, bone marrow involvement, and treatment response. A reduction in CD4+ PD-1 levels after treatment is associated with a trend towards improved overall survival.

## Linked entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133], CD274 (CD274 molecule) [NCBI Gene 29126]
- **Diseases:** non-Hodgkin lymphoma (MONDO:0018908)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 574058] {aka PDL1}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, PDCD1LG2 (programmed cell death 1 ligand 2) [NCBI Gene 574057] {aka PDL2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}, PDCD1 (programmed cell death 1) [NCBI Gene 100533201], TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, HLA-G (major histocompatibility complex, class I, G) [NCBI Gene 3135] {aka MHC-G}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** thrombocytopenia (MESH:D013921), bone marrow involvement (MESH:D001855), stage III-IV disease (MESH:D007676), SD (MESH:D060050), Cancer (MESH:D009369), infection (MESH:D007239), multiple myeloma (MESH:D009101), peripheral T-cell lymphoma (MESH:D016411), lung cancer (MESH:D008175), cytotoxic (MESH:D064420), LDH (MESH:C538133), anemia (MESH:D000740), chronic lymphocytic leukemia (MESH:D015451), hematological disorders (MESH:D006402), death (MESH:D003643), small cell lung cancer (MESH:D055752), neutropenia (MESH:D009503), cervical cancer (MESH:D002583), hematopoietic and lymphoid tissue tumors (MESH:D019337), congenital immunodeficiency (MESH:D000081207), DLBCL (MESH:D016403), infectious diseases (MESH:D003141), CR (MESH:D001766), cell (MESH:D002292), ITP (MESH:D016553), B-cell lymphoma (MESH:D016393), gastric cancer (MESH:D013274), thrombocytopenia:25.40 (OMIM:616433), PR (MESH:D004828), lymphoma (MESH:D008223), leukopenia (MESH:D007970), NHL (MESH:D008228), extranodal NK/T-cell lymphoma (MESH:D054391), aplastic anemia (MESH:D000741), PD (MESH:D018450), HL (MESH:D006689)
- **Chemicals:** Pembrolizumab (MESH:C582435), EDTA (MESH:D004492), rituximab (MESH:D000069283), vinblastine (MESH:D014747), brentuximab vedotin (MESH:D000079963), CHOP (-), doxorubicin (MESH:D004317), dacarbazine (MESH:D003606), anthracycline (MESH:D018943), bleomycin (MESH:D001761), Nivolumab (MESH:D000077594), gemcitabine (MESH:D000093542), methotrexate (MESH:D008727), ABVD (MESH:C034632)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935639/full.md

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Source: https://tomesphere.com/paper/PMC12935639