Evidence map›Paper›PMID 40099965›Full record

ArticleCancer research communications2025

Patients with Cervical Cancer with and without HIV Infection Have Unique T-cell Activation Profiles despite Similar Survival Outcomes after Chemoradiation.

Emily C MacDuffie, Luis Cocka, Xiang Lin, Memory Bvochora-Nsingo, Sebathu Chiyapo, Dawn Balang, Bokang Maswabi, Kebatshabile Ngoni, Doreen Ramogola-Masire, Nicola M Zetola and 5 more

Abstract read
In one paragraph

Article in Cancer research communications, 2025. 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

15 authors.

Emily C MacDuffie *Department of Radiation Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-8479-8512
Luis Cocka *Department of Microbiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0009-0005-6662-8911
Xiang LinDepartment of Computer Science, New Jersey Institute of Technology, Newark, New Jersey.ORCID 0000-0002-7634-5780
Memory Bvochora-NsingoDepartment of Oncology, Gaborone Private Hospital, Gaborone, Botswana.ORCID 0009-0008-9925-1286
Sebathu ChiyapoDepartment of Oncology, Sir Ketumile Masire Teaching Hospital, Gaborone, Botswana.ORCID 0000-0001-9800-1455
Dawn BalangDepartment of Oncology, Gaborone Private Hospital, Gaborone, Botswana.ORCID 0009-0001-6608-8397
Bokang MaswabiSchool of Medicine, University of Botswana, Gaborone, Botswana.ORCID 0000-0003-4699-5392
Kebatshabile NgoniSchool of Medicine, University of Botswana, Gaborone, Botswana.ORCID 0000-0002-2763-712X
Doreen Ramogola-MasireSchool of Medicine, University of Botswana, Gaborone, Botswana.ORCID 0000-0001-9624-8366
Nicola M ZetolaDepartment of Computer Science, New Jersey Institute of Technology, Newark, New Jersey.ORCID 0000-0003-0712-8579
Zhi WeiDepartment of Microbiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-6059-4267
Hao ShenDepartment of Microbiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-5003-4992
Sheynaz BassaDepartment of Radiation Oncology, University of Pretoria, Pretoria, South Africa.ORCID 0000-0001-5234-1577
Surbhi Grover *Department of Radiation Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-7443-5937
Erle S Robertson *Department of Otorhinolaryngology-Head and Neck Surgery, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-6088-2979

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROBERT GROSS · 1999 to 2026
$78.6M
Virus, Vector and Cell Culture CoreP01CA281867 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ERLE S. ROBERTSON · 2023 to 2026
$9.1M
Role of LANA-RBP-jk During Early KSHV InfectionP01CA174439 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2013 to 2018
$8.7M
Shared Resources CoreU54CA190158 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2014 to 2023
$4.2M
Tumor suppressor reprogramming by EBV through post-translational modificationR01CA268998 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2022 to 2025
$2.6M
Epigenetic Regulation of KSHV Genome ReplicationR01CA244074 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2019 to 2023
$2.5M
Genome Persistence of KSHVR01CA171979 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2013 to 2017
$1.5M
Prognostic value of quantitative HPV viral load in determining cervical cancer treatment response and recurrenceK08CA230170 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GROVER, SURBHI · 2019 to 2023
$1.4M
KSHV genome modification in KS tissueR01CA177423 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2013 to 2015
$594k
NCI NIH HHS K08 CA230170NCI NIH HHS P01 CA174439NCI NIH HHS P01 CA281867NCI NIH HHS R01 CA171979NCI NIH HHS R01 CA177423NCI NIH HHS R01 CA244074NCI NIH HHS R01 CA268998NCI NIH HHS U54 CA190158NIAID NIH HHS P30 AI045008
6 · The paper itself

Abstract

Abstract: The global burden of cervical cancer is highest in low- and middle-income countries. Women living with human immunodeficiency virus (HIV) infection are particularly affected by cervical cancer despite availability and adherence to antiretroviral therapy. Immune profile correlates of survival and treatment response have not been widely explored in patients with and without HIV infection. This study recruited women with cervical cancer undergoing definitive chemoradiation (CRT) in Botswana. Clinical characteristics and blood samples were collected. Flow cytometry was performed on samples prior to initiation, at completion, and 3 months after CRT. Logistic regression analysis identified immune markers that differed by HIV status and correlated with overall survival (OS). The study enrolled 131 consecutive women (HIV+ N = 89 and HIV− N = 42). From initiation to 3 months after CRT, a significant decrease in CD4 frequency (72%–60.55%, P < 0.001) and an increase in CD8 frequency (20.9%–31.5%, P < 0.001) were seen in women without HIV, whereas no significant changes in CD4 frequency (52.5%–50.9%) or CD8 frequency (39.9%–41.4%) were observed in those with HIV. Peripheral T cells underwent similar activation across the cohort regardless of HIV status. Improved OS was associated with reduced frequency of IL-2–expressing CD4 T-cell subsets. In women living with HIV, enhanced OS was associated with the presence of proinflammatory CD8 T cells. CRT induces peripheral T-cell activation and distinct cytokine profiles that differ by HIV status. Despite similar OS, HIV infection may differentially affect immune response to CRT in women with well-managed HIV. Significance: Chemoradiation affects the immune system of patients with cervical cancer with well-controlled HIV infection differently than those without HIV, yet their survival does not differ. This finding is an important step in understanding how management of HIV infection can modify cancer outcomes, particularly in settings with a high burden of HIV.

Indexed as

HIV InfectionsLymphocyte ActivationT-LymphocytesUterine Cervical NeoplasmsAdultChemoradiotherapyFemaleHumansMiddle AgedTreatment Outcome

Identifiers

PMID40099965
PMCPMC11995389

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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.