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General Commentary ARTICLE

Front. Psychiatry, 08 October 2015 | https://doi.org/10.3389/fpsyt.2015.00145

Commentary: The impact of neuroimmune alterations in autism spectrum disorder

  • 1Department of Experimental Medicine, Second University of Naples, Naples, Italy
  • 2Centre for Autism – La Forza del Silenzio, Caserta, Italy
  • 3Cancellautismo – No Profit Association for Autism Care, Florence, Italy

A commentary on

The impact of neuroimmune alterations in autism spectrum disorder
by Gottfried C, Bambini-Junior V, Francis F, Riesgo R and Savino W. (2015). Front. Psychiatry 6:121. doi:10.3389/fpsyt.2015.00121

The dramatic increasing prevalence of autism spectrum disorders (ASDs) (1), together with the influence on the quality of life and the lifetime societal cost of caring, has called for newest research on both the development of these diseases and the therapeutic options. Nowadays, it is well recognized that multifactorial and polygenic features (complex combination of genetic, epigenetic, and environmental interactions) characterize ASDs (2). Prenatal immune alterations and early inflammatory processes could be the autism etiological events. The authors Gottfried et al. (3) in this hypothesis-and-theory article discuss the recent findings in autism discovery. Starting from a brief historical way on autism development, the main topic of the article is to focus on the state-of-the-art of the novel findings in autism studies. The authors rightly highlight the newest challenging frontier of autism research: the neuroimmune axis alterations. These alterations are first evident in the cells early responsible for immune responses, as they are the precursors for macrophages, dendritic, and microglial cells: monocytes or peripheral blood mononuclear cells (PBMCs). These cells show strong dysfunctions in ASD children and are committed to a pro-inflammatory state, which in turn result in long-term immune alterations (4). In ASDs, altered PBMCs are responsible for elevated pro-inflammatory cytokine production. The up-regulation of inflammatory cytokines is also reflected in brain centers of autistic patients (5): the consequences are the induction of blood–brain barrier (the immunological interface between peripheral immune system and central nervous system) disruption. Changes in BBB permeability directly influence neural plasticity, connectivity and function, triggering impairments in social interaction, communication, and behavior (3). Immunological abnormalities also influence the gastrointestinal system and the microglial innate immune cells of the central nervous system (6). The authors also discuss the role of autoimmunity in the pathogenesis of autism. Familial or virus/bacteria-infected autoimmunity could be a risk factor for autism. Even if the exact cellular and molecular pathways responsible for the induction of neuroimmune alterations are still to be further clarify, a complex interaction among epigenetic and environmental risk factors (7) could trigger the neuroimmune abnormalities, such as abnormal neuron and glia responses.

Taken together, these autism-associated neuroimmune changes could help in identifying novel therapeutic target for a better future management of ASDs.

Conflict of Interest Statement

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

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Keywords: autism, neuroimmune interactions, epigenetics, monocytes, cytokines

Citation: Siniscalco D (2015) Commentary: The impact of neuroimmune alterations in autism spectrum disorder. Front. Psychiatry 6:145. doi: 10.3389/fpsyt.2015.00145

Received: 09 September 2015; Accepted: 22 September 2015;
Published: 08 October 2015

Edited by:

Kathleen Dave, St. Luke’s University Health Network, USA

Reviewed by:

Hongen Wei, Shanxi Medical University, China

Copyright: © 2015 Siniscalco. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Dario Siniscalco, dariosin@uab.edu