Evidence map›Paper›PMID 37787259›Full record

ArticleThe Indian journal of medical research2023

Normative data for paediatric lymphocyte subsets: A pilot study from western India.

Neha Jodhawat, Umair Ahmed Bargir, Priyanka Setia, Prasad Taur, Nidhi Bala, Aditi Madkaikar, Reetika Malik Yadav, Aparna Dalvi, Shweta Shinde, Maya Gupta and 7 more

Open access · diamondAbstract read
In one paragraph

Article in The Indian journal of medical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

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  7. Tregopathy in focus.Frontiers in immunology · 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

17 authors at 4 institutions in 1 country.

Neha JodhawatDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, aharashtra, India.
Umair Ahmed BargirDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
Priyanka SetiaDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
Prasad TaurDivision of Immunology, Bai Jerbai Wadia Hospital for Children, Nowrosjee Wadia Maternity Hospital, Mumbai, Maharashtra, India.
Nidhi BalaDepartment of Obstetrics & Gynaecology, Nowrosjee Wadia Maternity Hospital, Mumbai, Maharashtra, India.
Aditi MadkaikarDepartment of Biosciences & Bioengineering, Indian Institute of Technology, Guwahati, Assam, India.
Reetika Malik YadavDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
Aparna DalviDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
Shweta ShindeDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
Maya GuptaDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
Shraddha ShelarDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
Priyanka KambliDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
Vijaya GowriDivision of Immunology, Bai Jerbai Wadia Hospital for Children, Nowrosjee Wadia Maternity Hospital, Mumbai, Maharashtra, India.
Madhukar LokeshwarDepartment of Paediatrics, Kashyap Nursing Home, Mumbai, Maharashtra, India.
Purnima SatoskarDepartment of Obstetrics & Gynaecology, Nowrosjee Wadia Maternity Hospital, Mumbai, Maharashtra, India.
Mukesh DesaiDivision of Immunology, Bai Jerbai Wadia Hospital for Children, Nowrosjee Wadia Maternity Hospital, Mumbai, Maharashtra, India.
Manisha MadkaikarDepartment of Pediatric Immunology & Leukocyte Biology, Indian Council of Medical Research - National Institute of Immunohaematology, KEM Hospital, Mumbai, Maharashtra, India.
National Institute of Immunohaematology · INBai Jerbai Wadia Hospital for Children · INDr. BMN College of Home Science · INIndian Institute of Technology Guwahati · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & objectives: Accurate diagnosis of immunodeficiencies requires a critical comparison of values with age-matched controls. In India, the existing reference values for rare lymphocyte subsets are currently not available and we rely on the data originating from other countries for the interpretation of the results. Furthermore, there is limited information on normal variation for these rare-subset parameters in Indian children. So, this study aimed to establish normative values for clinically important lymphocyte subsets in Indian children at different age groups. Methods: 148 children aged ≥16 yr were enrolled in this study. The study population included 61 per cent males and 39 per cent females and was divided into the following groups: cord blood (n=18), 0-6 months (n=9), 6-12 months (n=13), 1-2 yr (n=19), 2-5 yr (n=27), 5-10 yr (n=25) and 10-16 yr (n=37). The absolute and relative percentage of lymphocytes, T, B, natural killer cell, along with activated, naïve and memory subsets, was determined by flow cytometry. Results: Median values and the 10 Interpretation & conclusions: This single-centre pilot study provides preliminary data that justifies the need for future large-scale multi centric studies to generate a reference range for interpreting extended immunophenotyping profiles in the paediatric age group, making it possible for clinicians to assess the immunological status in inborn errors of immunity, infectious and autoimmune diseases.

Indexed as

Lymphocyte SubsetsT-Lymphocyte SubsetsChildFemaleFlow CytometryHumansImmunophenotypingIndiaLymphocyte CountMalePilot ProjectsReference ValuesChildrenflow cytometrylymphocyte subsetpilot studyprimary immunodeficiency

Identifiers

PMID37787259
PMCPMC10645029
OpenAlexW4387296200

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LicenceCC BY-NC-SA
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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.