Evidence map›Paper›PMID 36604576›Full record

ArticleScientific reports2023

Long-term presence of autoantibodies in plasma of cured leprosy patients.

Xi Yang, Hua Dong, Yi-Qun Kuang, Xiu-Feng Yu, Heng Long, Chun-Yu Zhang, Dong Wang, Deng-Feng Zhang, Yu-Ye Li

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 24% of its field
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Understanding Autoimmune Response Mechanisms in Leprosy.Indian dermatology online journal · 2025
    Article
  6. Article
  7. The research progress of LACC1.Frontiers in immunology · 2025
    Review
  8. Article
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

9 authors at 4 institutions in 1 country.

Xi Yang *Department of Dermatology, First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, China.
Hua Dong *Department of Dermatology, First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, China.
Yi-Qun Kuang *NHC Key Laboratory of Drug Addiction Medicine, First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, China.
Xiu-Feng YuWenshan Institute of Dermatology, Wenshan, 663000, Yunnan, China.
Heng LongWenshan Institute of Dermatology, Wenshan, 663000, Yunnan, China.
Chun-Yu ZhangWenshan Institute of Dermatology, Wenshan, 663000, Yunnan, China.
Dong WangKey Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences and Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650223, Yunnan, China.
Deng-Feng ZhangKey Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences and Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650223, Yunnan, China. zhangdengfeng@mail.kiz.ac.cn.
Yu-Ye LiDepartment of Dermatology, First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, China. yyeli2000@126.com.
Wenshan University · CNChinese Academy of Sciences · CNFirst Affiliated Hospital of Kunming Medical University · CNKunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoantibodies have been detected in leprosy patients, indicating that infection with M. leprae may lead to autoimmune disorders. However, whether autoimmune response last until patients are cured is unknown. Knowing the autoimmune response in cured leprosy patients is essential to identify whether symptoms are caused by leprosy itself or by other immune-related diseases. This knowledge is essential for the ongoing health management in cured leprosy patients where autoimmune disorders still exist. In our study, we selected six autoantibodies, including anticardiolipin antibody of IgG (ACA), anti-nuclear antibody (ANA), extractable nuclear antigen antibody (ENA), anti-streptolysin O (ASO), anti-double stranded DNA antibody (dsDNA), and rheumatoid factor (RF), that had been reported in leprosy patients as typical autoantibodies. We tested the six typical autoantibodies combined with LACC1, which encodes a protein associated with autoimmune disease such as Crohn's disease and is also the susceptible gene conferring leprosy risk, in cured leprosy patients through ELISA to assess the cured patient's immune status. We observed high positive rates of autoantibodies in cured leprosy patients, and the average plasma levels of five (ACA, ANA, ENA, ASO, and RF) out of the six autoantibodies were significantly higher in cured leprosy patients than in controls. The positive detection of autoantibodies is independent of the recovery period. Moreover, the level of these autoantibodies showed a strong positive correlation with the level of LACC1 in both controls and cured patients. This study showed that there is long-term autoimmunological activation in leprosy patients, even after decades of recovery. Autoimmune responses may influence the development and prognosis of leprosy. Special care should be given to posttreatment or cured leprosy patients regarding long-term autoimmunological activation.

Indexed as

Autoimmune DiseasesLeprosyAntibodies, AntinuclearAutoantibodiesHumansMycobacterium lepraeRheumatoid FactorAntibodies, AntinuclearAutoantibodiesRheumatoid Factor

Identifiers

PMID36604576
PMCPMC9816311
OpenAlexW4313563762

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Registered trials

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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.