@article{a4e6e0b08f4a46b2973fd2fc3154377a,
title = "Etiology of breast implant-associated anaplastic large cell lymphoma (Bia-alcl): Current directions in research",
abstract = "Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is a CD30-positive, anaplastic lymphoma kinase-negative T-cell lymphoma. Where implant history is known, all confirmed cases to date have occurred in patients with exposure to textured implants. There is a spectrum of disease presentation, with the most common occurring as a seroma with an indolent course. A less common presentation occurs as locally advanced or, rarely, as metastatic disease. Here we review the immunological characteristics of BIA-ALCL and potential triggers leading to its development. BIA-ALCL occurs in an inflammatory microenvironment with significant lymphocyte and plasma cell infiltration and a prominent Th1/Th17 phenotype in advanced disease. Genetic lesions affecting the JAK/STAT signaling pathway are commonly present. Proposed triggers for the development of malignancy include mechanical friction, silicone implant shell particulates, silicone leachables, and bacteria. Of these, the bacterial hypothesis has received significant attention, supported by a plausible biologic model. In this model, bacteria form an adherent biofilm in the favorable environment of the textured implant surface, producing a bacterial load that elicits a chronic inflammatory response. Bacterial antigens, primarily of Gram-negative origin, may trigger innate immunity and induce T-cell proliferation with subsequent malignant transformation in genetically susceptible individuals. Although much remains to be elucidated regarding the multifactorial origins of BIA-ALCL, future research should focus on prevention and treatment strategies, recognizing susceptible populations, and whether decreasing the risk of BIA-ALCL is possible.",
keywords = "Antigens, Bacterial, Breast implants, Lymphoma, T-cells",
author = "Deva, {Anand K.} and Turner, {Suzanne D.} and Kadin, {Marshall E.} and Magnusson, {Mark R.} and Prince, {H. Miles} and Miranda, {Roberto N.} and Inghirami, {Giorgio G.} and Adams, {William P.}",
note = "Funding Information: and the poorer prognosis infiltrative and metastatic BIA-ALCL. Development of an experimental developed line of research supports the bacterial hypothesis by which biofilm elicits an inflammatory immune response, eventually resulting in malignant transformation of cells. Among the many unknowns are the specific antigen or superantigen involved, detailed pathways to transformation, particular genetic factors associated with an increased risk of BIA-ALCL, and possible change in classification to lymphoproliferative disorder or possible differences in etiology between effusion-Critical Review of Manuscript for Important Intellectual Contributions: A.K.D., S.D.T., M.E.K., M.R.M., H.M.P., limited BIA-ALCL and the poorer prognosis infiltrative and metastatic BIA-ALCL. Development of an experimental animal model and ongoing translational and clinical research will further elucidate Funding: This research was funded by Allergan plc, Dublin, Ireland (prior to its acquisition by AbbVie). the pathobiology and guide the avoidance and treatment of this disease. Acknowledgments: Writing and editorial assistance was provided to the authors by Robert Rydzewski, CMPP, of Peloton Advantage, LLC, an Open Health company, Parsippany, NJ, and was funded by Allergan plc, Author Contributions: Review Concept and Design: A.K.D., S.D.T., M.R.M., H.M.P. Expert Opinion: . A.K.D., Dublin, Ireland (prior to its acquisition by AbbVie). Neither honoraria nor other forms of payment were made S.D.T., M.E.K., M.R.M., H.M.P., R.N.M., G.G.I., W.P.A.J. Drafting of Manuscript: A.K.D., S.D.T., M.R.M., H.M.P. Critical Review of Manuscript for Important Intellectual Contributions: A.K.D., S.D.T., M.E.K., M.R.M., H.M.P., Conflicts of Interest: Drs. Turner and Inghirami have no financial disclosures. Dr. Adams has received research R.N.M., G.G.I., W.P.A.J. All authors have read and agreed to the published version of the manuscript. grants from the Aesthetic Society Education and Research Foundation and is an unpaid education advisor for Allergan and Sientra. Professor Deva is a consultant and research coordinator for Allergan, Mentor (J&J), Sientra, and Motiva (Establishment Labs). Professor Prince is a paid consultant to and receives research support from TAackkendoawPlheadrgmmaecenutst:icWalrsi,tiMngil laenndn eiudmitoPrihaal ramssaiscteauntciecawlsaas npdroAvlildeerdgaton.thDer .auKtahdoirns rbeyc eRivobeserrte Rseyadrczhewsuskpip,C oMrt PfrPo,m of Peloton Advantage, LLC, an Open Health company, Parsippany, NJ, and was funded by Allergan plc, Dublin, Publisher Copyright: {\textcopyright} 2020 by the authors. Licensee MDPI, Basel, Switzerland.",
year = "2020",
month = dec,
doi = "10.3390/cancers12123861",
language = "English (US)",
volume = "12",
pages = "1--14",
journal = "Cancers",
issn = "2072-6694",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "12",
}