Evidence map›Paper›PMID 33487699›Full record

ArticleIndian journal of dermatology

Immune Responses in Post Kala-azar Dermal Leishmaniasis.

Mitali Chatterjee, Ritika Sengupta, Debanjan Mukhopadhyay, Shibabrata Mukherjee, Aishwarya Dighal, Srija Moulik, Shilpa Sengupta

Open access · diamondAbstract read
In one paragraph

Article in Indian journal of dermatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 25% 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, 13 citations in OpenAlex.

  1. Trial
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  6. Commentary on the Issue ofVeterinary sciences · 2025
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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

7 authors at 1 institution in 1 country.

Mitali ChatterjeeDepartment of Pharmacology, Institute of Postgraduate Medical Education and Research, Kolkata, West Bengal, India.
Ritika SenguptaDepartment of Pharmacology, Institute of Postgraduate Medical Education and Research, Kolkata, West Bengal, India.
Debanjan MukhopadhyayDepartment of Pharmacology, Institute of Postgraduate Medical Education and Research, Kolkata, West Bengal, India.
Shibabrata MukherjeeDepartment of Pharmacology, Institute of Postgraduate Medical Education and Research, Kolkata, West Bengal, India.
Aishwarya DighalDepartment of Pharmacology, Institute of Postgraduate Medical Education and Research, Kolkata, West Bengal, India.
Srija MoulikDepartment of Pharmacology, Institute of Postgraduate Medical Education and Research, Kolkata, West Bengal, India.
Shilpa SenguptaDepartment of Pharmacology, Institute of Postgraduate Medical Education and Research, Kolkata, West Bengal, India.
Institute of Post Graduate Medical Education and Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kala-azar, commonly known as visceral leishmaniasis (VL), is a neglected tropical disease that has been targeted in South Asia for elimination by 2020. Presently, the Kala-azar Elimination Programme is aimed at identifying new low-endemic foci by active case detection, consolidating vector control measures, and decreasing potential reservoirs, of which Post Kala-azar Dermal Leishmaniasis (PKDL) is considered as the most important. PKDL is a skin condition that occurs after apparently successful treatment of VL and is characterized by hypopigmented patches (macular) or a mixture of papules, nodules, and/or macules (polymorphic). To achieve this goal of elimination, it is important to delineate the pathophysiology so that informed decisions can be made regarding the most appropriate and cost-effective approach. We reviewed the literature with regard to PKDL in Asia and Africa and interpreted the findings in establishing a potential correlation between the immune responses and pathophysiology. The overall histopathology indicated the presence of a dense, inflammatory cellular infiltrate, characterized by increased expression of alternatively activated CD68+ macrophages, CD8+ T cells showing features of exhaustion, CD20+ B cells, along with decreased CD1a+ dendritic cells. Accordingly, this review is an update on the overall immunopathology of PKDL, so as to provide a better understanding of host-parasite interactions and the immune responses generated which could translate into availability of markers that can be harnessed for assessment of disease progression and improvement of existing treatment modalities.

Indexed as

Immune responsekala-azarpost kala-azar dermal leishmaniasisvisceral leishmaniasis

Identifiers

PMID33487699
PMCPMC7810083
OpenAlexW3093834667

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.