Multidisciplinary approach to treating complex immune dysregulation disorders: an adaptive model for institutional implementation
- PMID: 40124385
- PMCID: PMC11926151
- DOI: 10.3389/fimmu.2025.1519955
Multidisciplinary approach to treating complex immune dysregulation disorders: an adaptive model for institutional implementation
Abstract
Patients with immune dysregulation may present with varying combinations of autoimmunity, autoinflammation, immunodeficiency, atopy, lymphoproliferation, and/or malignancy, often with multisystem involvement. Recognizing specific patterns of immune dysregulation, coordinating and interpreting complex diagnostic testing, and choosing initial (often empiric) treatment can be challenging. Centers are increasingly assembling multidisciplinary teams (MDTs) to standardize evaluation and optimize treatment of patients with complex immune dysregulation (immune dysregulation MDTs [immMDTs]). However, published information on the composition and function of immMDTs is sparse, and there is little guidance for those seeking to establish or optimize an immMDT. To inform this review, we assembled a panel of 24 pediatric providers from multiple specialties who actively participate in immMDTs to provide expert opinion. We also conducted a search of the available information on pediatric immMDTs from PubMed. Based on these insights, we summarize the structure and function of active immMDTs across the United States and focus on best practices and context-dependent solutions that may enable institutions with varying goals, patient populations, and resources to establish an immMDT.
Keywords: collaborative management; hemophagocytic lymphohistiocytosis; immune dysregulation; institutional implementation; multidisciplinary teams; quality improvement research.
Copyright © 2025 Henderson, Abraham, Ahmed, Blount, Canna, Chaimowitz, Chandrakasan, Coates, Connelly, Cooper, Duncan, French, Hazen, Hermiston, Nolan, Ray, Rose, Satter, Schulert, Tejtel, Vogel, Walkovich, Zinter and Behrens.
Conflict of interest statement
LAH received salary support from CARRA; investigator-initiated research grants from BMS; and consulting fees from Sobi, Pfizer, and Adaptive Biotechnologies. RSA, AA, NSC, MAC, SC, CND, AF, MH, SKST, KW, and MSZ have nothing to disclose. LB has participated in a medical advisory board and served as a consultant for Sobi. SWC received consulting fees from Sobi. BC is funded by NHLBI and the American Lung Association. JAC has served on advisory boards for Sobi and Pharming. MLH has served on external advisory boards for Novartis and Sobi. BN has participated in a medical advisory board for Sobi. AR serves as a speaker/advisor for Sobi and BTG. MJR has served on advisory boards for Genentech and Novartis. LFS has served as a consultant for Grifols, Takeda, CSL Behring, Horizon, Sobi, and Pharming. GS has received consulting fees from Boehringer Ingelheim and research support from IpiNovyx. TV has consulted for Novartis, Sobi, Pfizer, and Moderna and receives research support from AstraZeneca. EMB has consulted for and received grant support from Sobi. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The authors declare that this study received funding from Sobi, Inc. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
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