Evidence map›Paper›PMID 34582592›Full record

ArticleImmunology and cell biology2022

Comprehensive immune cell profiling depicts an early immune response associated with severe coronavirus disease 2019 in cancer patients.

Prashant R Tembhare, Harshini Sriram, Gaurav Chatterjee, Twinkle Khanka, Anant Gokarn, Sumeet Mirgh, Akhil Rajendra, Anumeha Chaturvedi, Sitaram G Ghogale, Nilesh Deshpande and 17 more

Abstract read
In one paragraph

Article in Immunology and cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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  5. Review
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

27 authors.

Prashant R TembhareHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.ORCID 0000-0002-9030-0415
Harshini SriramHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Gaurav ChatterjeeHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Twinkle KhankaHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Anant GokarnDepartment of Medical Oncology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Sumeet MirghDepartment of Medical Oncology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Akhil RajendraDepartment of Medical Oncology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Anumeha ChaturvediHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Sitaram G GhogaleHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Nilesh DeshpandeHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Karishma GiraseHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Kajal DalviHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Sweta RajpalHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Nikhil PatkarHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Bhakti TrivediDepartment of Anesthesiology, Critical Care and Pain, Tata Memorial Center, HBNI University, Mumbai, India.
Amit JoshiDepartment of Medical Oncology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Vedang MurthyDepartment of Radiation Oncology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Nitin ShettyDepartment of Radio-Diagnosis, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Sudhir NairDepartment of Head and Neck Surgical Oncology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Ashwini MoreDepartment of Medicine, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Sujeet KamtalwarDepartment of Medicine, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Preeti ChavanComposite Laboratory and Microbiology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Vivek BhatComposite Laboratory and Microbiology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Prashant BhatMedical Administration, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Papagudi G SubramanianHematopathology Laboratory, ACTREC, Tata Memorial Center, Homi Bhabha National Institute (HBNI) University, Mumbai, India.
Sudeep GuptaDepartment of Medical Oncology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.
Navin KhattryDepartment of Medical Oncology, ACTREC, Tata Memorial Center, HBNI University, Mumbai, India.

Funding

Advanced Centre for Treatment, Research and Education in Cancer (ACTREC) Intramural
6 · The paper itself

Abstract

Recent studies have highlighted multiple immune perturbations related to severe acute respiratory syndrome coronavirus 2 infection-associated respiratory disease [coronavirus disease 2019 (COVID-19)]. Some of them were associated with immunopathogenesis of severe COVID-19. However, reports on immunological indicators of severe COVID-19 in the early phase of infection in patients with comorbidities such as cancer are scarce. We prospectively studied about 200 immune response parameters, including a comprehensive immune-cell profile, inflammatory cytokines and other parameters, in 95 patients with COVID-19 (37 cancer patients without active disease and intensive chemo/immunotherapy, 58 patients without cancer) and 21 healthy donors. Of 95 patients, 41 had severe disease, and the remaining 54 were categorized as having a nonsevere disease. We evaluated the association of immune response parameters with severe COVID-19. By principal component analysis, three immune signatures defining characteristic immune responses in COVID-19 patients were found. Immune cell perturbations, in particular, decreased levels of circulating dendritic cells (DCs) along with reduced levels of CD4 T-cell subsets such as regulatory T cells (T

Indexed as

COVID-19NeoplasmsHumansImmunitySARS-CoV-2T-Lymphocyte SubsetsCancer patientsCOVID-19immune cell profileinflammatory cytokinesmyeloid dendritic cellsSARS-CoV-2severe disease

Identifiers

PMID34582592
PMCPMC8652640

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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.