Evidence map›Paper›PMID 37342323›Full record

ReviewFrontiers in immunology2023

Immune-related adverse effects of checkpoint immunotherapy and implications for the treatment of patients with cancer and autoimmune diseases.

Betul Ibis, Konstantinos Aliazis, Carol Cao, Sasitorn Yenyuwadee, Vassiliki A Boussiotis

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
15.2field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
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  11. Imaging Immunotherapy.Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer · 2026
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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

5 authors at 2 institutions in 1 country.

Betul IbisDivision of Hematology-Oncology Beth Israel Deaconess Medical Center, Boston, MA, United States.
Konstantinos AliazisDivision of Hematology-Oncology Beth Israel Deaconess Medical Center, Boston, MA, United States.
Carol CaoDivision of Hematology-Oncology Beth Israel Deaconess Medical Center, Boston, MA, United States.
Sasitorn YenyuwadeeDivision of Hematology-Oncology Beth Israel Deaconess Medical Center, Boston, MA, United States.
Vassiliki A BoussiotisDivision of Hematology-Oncology Beth Israel Deaconess Medical Center, Boston, MA, United States.
Beth Israel Deaconess Medical Center · USHarvard University · US

Funding

Advancing Treatment Outcomes in Malignant Glioma by Integrating Immunotherapy and Standard of Care using Genetically Engineered Mice that Recapitulate Molecular Feature of Human GliomaR01CA229784 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUSSIOTIS, VASSILIKI A, CHAREST, ALAIN · 2018 to 2022
$3.3M
The effects of PD-1 on tumor-mediated “emergency” myelopoiesis and fate commitment of myeloid cells: Implications for anti-tumor immunityR01CA238263 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUSSIOTIS, VASSILIKI A · 2020 to 2024
$3.1M
Detection of PD-1 inhibitory signaling and its molecular relays in T cells: Implications for cancer immunotherapyR01CA257672 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI VASSILIKI A BOUSSIOTIS, Ioannis Vlachos · 2023 to 2026
$2.8M
Understanding the cellular and functional changes in the immune tumor microenvironment of glioblastoma during progression and treatments.R01CA271601 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI VASSILIKI A BOUSSIOTIS, Alain Charest · 2023 to 2026
$2.6M
NCI NIH HHS R01 CA229784NCI NIH HHS R01 CA238263NCI NIH HHS R01 CA257672NCI NIH HHS R01 CA271601
6 · The paper itself

Abstract

During the past decade, there has been a revolution in cancer therapeutics by the emergence of antibody-based immunotherapies that modulate immune responses against tumors. These therapies have offered treatment options to patients who are no longer responding to classic anti-cancer therapies. By blocking inhibitory signals mediated by surface receptors that are naturally upregulated during activation of antigen-presenting cells (APC) and T cells, predominantly PD-1 and its ligand PD-L1, as well as CTLA-4, such blocking agents have revolutionized cancer treatment. However, breaking these inhibitory signals cannot be selectively targeted to the tumor microenvironment (TME). Since the physiologic role of these inhibitory receptors, known as immune checkpoints (IC) is to maintain peripheral tolerance by preventing the activation of autoreactive immune cells, IC inhibitors (ICI) induce multiple types of immune-related adverse effects (irAEs). These irAEs, together with the natural properties of ICs as gatekeepers of self-tolerance, have precluded the use of ICI in patients with pre-existing autoimmune diseases (ADs). However, currently accumulating data indicates that ICI might be safely administered to such patients. In this review, we discuss mechanisms of well established and newly recognized irAEs and evolving knowledge from the application of ICI therapies in patients with cancer and pre-existing ADs.

Indexed as

Antineoplastic Agents, ImmunologicalAutoimmune DiseasesDrug-Related Side Effects and Adverse ReactionsNeoplasmsAntibodies, MonoclonalHumansImmunotherapyTumor MicroenvironmentAntibodies, MonoclonalAntineoplastic Agents, Immunologicalautoimmune diseasecancerImmune checkpoint inhibitors (ICIs)immune-related adverse events (irAEs)immunotherapy

Identifiers

PMID37342323
PMCPMC10277501
OpenAlexW4379386535

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.