Inflammation identity crisis: pathogenic nature of platelet-derived transforming growth factor β in chronic inflammatory conditions
Year: 2026
Type: review
Abstract: Chronic inflammatory conditions are associated with sustained platelet activation and subsequent release of platelet-derived immunomodulatory factors. Among these, platelets are the largest circulating reservoir of transforming growth factor β (TGFβ), and as such can be implicated in all physiological processes where TGFβ plays a crucial role. TGFβ is associated with immune regulation via dampening of Th 1 responses, amplification of regulatory T lymphocyte polarization, and reduced inflammation, which can be beneficial in mitigating autoimmune diseases. However, in the case of solid tumors or persistent viral infections, this function can result in aberrant immune suppression and increased disease severity and pathology. TGFβ is also implicated in tissue remodeling and wound healing, however, in conditions associated with chronic platelet activation, such as diabetes, hypertension, and HIV infection, increased levels of platelet-derived TGFβ can exacerbate fibrosis, resulting in tissue and organ damage. Thus, whether TGFβ plays a pathogenic or pro-homeostatic role is dependent on the disease context. In order to harness the therapeutic potential of platelet-derived TGFβ, it is crucial to first understand how its mechanism of action varies across physiologic and pathologic conditions. In this review, we aim to emphasize the highly pleiotropic nature of TGFβ, highlight what is currently known about platelet-derived TGFβ across disease states, and to reinforce the importance of considering platelet-derived mediators as regulators of immunity and tissue responses, especially in the presence of chronic inflammation.
Source: Frontiers in Immunology
Institutions: University of Rochester Medicine, University of Rochester
Language: English
Topic: TGF-β signaling in diseases
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,801
Awards: G2021609668, Platelet-medicated deregulation of dendritic cell function- implications for anti-HIV immune responses and immunotherapy, Role of platelet- monocyte interaction in promoting pro-atherogenic state in HIV-infected individuals, The T32 Predoctoral Training Program in Immunology (PTPI)
OpenAlex ID: W7220469356