Evidence map›Paper›PMID 42162342›Full record

ArticleClinical and experimental medicine2026

Tacrolimus has better performance in B cell reconstitution after allo-HSCT compared to cyclosporine A: a real-world study.

Hao Zhou, Guangyu Zhou, Wenqiong Xiang, Guilin Ren, Xi Dou, Jianbin Chen, Xiaoqiong Tang, Hongbin Zhang, Xin Wang, Xiaohua Luo and 2 more

Abstract readComparative Study
In one paragraph

Article in Clinical and experimental medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Hao Zhou *Department of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Guangyu Zhou *Department of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Wenqiong XiangDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Guilin RenDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Xi DouDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Jianbin ChenDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Xiaoqiong TangDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Hongbin ZhangDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Xin WangDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Xiaohua LuoDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Lin LiuDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Li WangDepartment of Hematology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China. liwang@hospital.cqmu.edu.cn.ORCID http://orcid.org/0000-0001-7692-5067

Funding

Chongqing Medical University W0193Natural Science Foundation Project of Chongqing, Chongqing Science and Technology Commission CSTB2024NSCQ-KJFZZDX0021
6 · The paper itself

Abstract

B-cell reconstitution is closely associated with prognosis, infection risk, and graft-versus-host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, the impact of different calcineurin inhibitors (CNIs) on B-cell recovery remains unclear. We retrospectively analyzed 312 allo-HSCT recipients receiving cyclosporine (CsA, n = 211) or tacrolimus (FK506, n = 101). B-cell proportions in bone marrow and peripheral lymphocyte subsets were compared, and propensity score matching was applied to balance confounders. Multivariate analysis demonstrated that FK506 was independently associated with superior B-cell reconstitution at 3 months (OR 2.93, 95% CI 1.49-5.76, p = 0.010) and 4 months post-transplant (OR 3.53, 95% CI 1.11-11.15, p = 0.024). Higher B-cell proportions at 3-5 months were associated with a significantly lower risk of viral infection. Mediation analysis further revealed that improved B-cell reconstitution at day + 90 partially mediated the protective effect of FK506 against viral infection. These findings suggest that FK506 promotes improved B-cell recovery and may reduce viral infection risk after allo-HSCT.

Indexed as

B-LymphocytesCalcineurin InhibitorsCyclosporineHematopoietic Stem Cell TransplantationImmune ReconstitutionImmunosuppressive AgentsTacrolimusAdultFemaleGraft vs Host DiseaseHumansMaleMiddle AgedRetrospective StudiesTransplantation, HomologousCalcineurin InhibitorsCyclosporineImmunosuppressive AgentsTacrolimusAllo-HSCTB cellsCalcineurin inhibitorGlucocorticoidImmune reconstitution

Identifiers

PMID42162342
PMCPMC13356079

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.