Efficacy and advantage of immunotherapy for melanoma via intramuscular co-expression of plasmid-encoded PD-1 and CTLA-4 scFvs DOI
Yueyao Yang, Qian Huang,

Mo Cheng

et al.

American Journal of Cancer Research, Journal Year: 2024, Volume and Issue: 14(5), P. 2626 - 2642

Published: Jan. 1, 2024

Immunotherapy, in the shape of immune checkpoint inhibitors (ICIs), has completely changed treatment cancer. However, increasing expense and frequency immune-related side effects, which are frequently associated with combination antibody therapies Fc fragment antibody, have limited patient's ability to benefit from these treatments. Herein, we presented therapeutic effects plasmid-encoded PD-1 CTLA-4 scFvs (single-chain variable fragment) for melanoma

Language: Английский

Human organoids with an autologous tissue-resident immune compartment DOI Creative Commons
Timothy Recaldin, Linda Steinacher,

Bruno Gjeta

et al.

Nature, Journal Year: 2024, Volume and Issue: 633(8028), P. 165 - 173

Published: Aug. 14, 2024

The intimate relationship between the epithelium and immune system is crucial for maintaining tissue homeostasis, with perturbations therein linked to autoimmune disease cancer

Language: Английский

Citations

31

Gut microbiome and immune checkpoint inhibitor toxicity DOI Creative Commons
Rik J. Verheijden, Mick J M van Eijs, Fernanda L. Paganelli

et al.

European Journal of Cancer, Journal Year: 2025, Volume and Issue: 216, P. 115221 - 115221

Published: Jan. 5, 2025

Language: Английский

Citations

3

CTLA-4-expressing ILC3s restrain interleukin-23-mediated inflammation DOI

Anees Ahmed,

Ann Mary Joseph, Jordan Zhou

et al.

Nature, Journal Year: 2024, Volume and Issue: 630(8018), P. 976 - 983

Published: June 12, 2024

Language: Английский

Citations

14

Novel strategies for modulating the gut microbiome for cancer therapy DOI
Young Seok Cho, Kai Han,

Jin Xu

et al.

Advanced Drug Delivery Reviews, Journal Year: 2024, Volume and Issue: 210, P. 115332 - 115332

Published: May 15, 2024

Language: Английский

Citations

11

Leveraging dirty mice that have microbial exposure to improve preclinical models of human immune status and disease DOI

Qian Liu,

Thames Pickett,

Deborah L. Hodge

et al.

Nature Immunology, Journal Year: 2024, Volume and Issue: 25(6), P. 947 - 950

Published: May 15, 2024

Language: Английский

Citations

6

Recent advances in understanding the immune microenvironment in ovarian cancer DOI Creative Commons
Jinxin Chen, Lu Yang, Yiming Ma

et al.

Frontiers in Immunology, Journal Year: 2024, Volume and Issue: 15

Published: June 5, 2024

The occurrence of ovarian cancer (OC) is a major factor in women’s mortality rates. Despite progress medical treatments, like new drugs targeting homologous recombination deficiency, survival rates for OC patients are still not ideal. tumor microenvironment (TME) includes cells, fibroblasts linked to (CAFs), immune-inflammatory and the substances these cells secrete, along with non-cellular components extracellular matrix (ECM). First, TME mainly plays role inhibiting growth protecting normal cell survival. As tumors progress, gradually becomes place promote progression. Immune have attracted much attention as targets immunotherapy. checkpoint inhibitor (ICI) therapy has potential regulate TME, suppressing factors that facilitate advancement, reactivating immune managing growth, extending advanced cancer. This review presents an outline current studies on distinct cellular elements within detailing their main functions possible signaling pathways. Additionally, we examine immunotherapy rechallenge OC, specific emphasis biological reasons behind resistance ICIs.

Language: Английский

Citations

4

Integrating natural commensals and pathogens into preclinical mouse models DOI
Barbara Rehermann, Andrea L. Graham, David Masopust

et al.

Nature reviews. Immunology, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 19, 2024

Language: Английский

Citations

4

Commensal fungi, a force to be reckoned with DOI
Dingjiacheng Jia,

Shujie Chen

Cell Host & Microbe, Journal Year: 2025, Volume and Issue: 33(1), P. 6 - 8

Published: Jan. 1, 2025

Language: Английский

Citations

0

The Gut Microbiota‐Xanthurenic Acid‐Aromatic Hydrocarbon Receptor Axis Mediates the Anticolitic Effects of Trilobatin DOI Creative Commons
Xiaoyu Wu,

Jiajia Wei,

Ran Wang

et al.

Advanced Science, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 21, 2025

Abstract Current treatments for ulcerative colitis (UC) remain limited, highlighting the need novel therapeutic strategies. Trilobatin (TLB), a naturally derived food additive, exhibits potential anti‐inflammatory properties. In this study, dextran sulfate sodium (DSS)‐induced animal model is used to investigate effects of TLB on UC. It found significantly alleviates DSS‐induced UC in mice, as evidenced by reduction disease activity index, an increase colon length, improvement histopathological lesions. Furthermore, treatment results decrease proinflammatory cytokines and cytokines. mitigates modulating intestinal microbiota, particularly Akkermansia , which enhances tryptophan metabolism upregulates production xanthurenic acid (XANA). To confirm role TLB‐induced microbiota changes, experiments are performed with pseudogerm‐free mice fecal transplantation. also identified XANA key metabolite that mediates TLB's protective effects. Both markedly activate aromatic hydrocarbon receptor (AhR). Administration AhR antagonist abrogates their effects, thereby confirming involvement underlying mechanism. conclusion, study reveals mechanism through correcting imbalances, regulating metabolism, enhancing production, activating AhR.

Language: Английский

Citations

0

Improving bench-to-bedside translation for acute graft-versus-host disease models DOI Creative Commons

Brianyell McDaniel Mims,

Kathryn L. Furr,

Josue Enriquez

et al.

Disease Models & Mechanisms, Journal Year: 2025, Volume and Issue: 18(2)

Published: Feb. 1, 2025

ABSTRACT The transplantation of allogeneic hematopoietic stem cells is a potentially curative treatment for hematological malignancies, inherited blood disorders and immune deficiencies. Unfortunately, 30-50% patients receiving will develop life-threatening inflammatory disease called acute graft-versus-host (aGVHD). In with aGVHD, graft-associated T cells, which typically target the skin, intestinal tract liver, can also damage lungs lymphoid tissue. Damage to tissue creates prolonged immunodeficiency that markedly increases risk infections bleeding, resulting in considerable morbidity mortality. Although mouse models aGVHD have been instrumental our understanding this condition's pathogenesis, translation preclinical data into new more effective treatments human has limited reasons remain be fully understood. However, evidence suggests factors associated likely contribute these unsatisfactory results. Review, we identify discuss specific inherent may limit patient treatment, suggest how improve translatability models.

Language: Английский

Citations

0