Reduced Follicular Regulatory T Cells in Spleen and Pancreatic Lymph Nodes of Patients With Type 1 Diabetes

Author:

Vecchione Andrea12,Jofra Tatiana1,Gerosa Jolanda1,Shankwitz Kimberly3,Di Fonte Roberta1,Galvani Giuseppe1,Ippolito Elio1,Cicalese Maria Pia456,Schultz Andrew R.7,Seay Howie R.7,Favellato Mariagrazia1,Milardi Giulia1,Stabilini Angela1,Ragogna Francesca1,Grogan Pauline89,Bianconi Eleonora89,Laurenzi Andrea8,Caretto Amelia8,Nano Rita1,Melzi Raffaela1,Danzl Nichole2,Bosi Emanuele1689,Piemonti Lorenzo168,Aiuti Alessandro456,Brusko Todd710,Petrovas Constantinos3,Battaglia Manuela19,Fousteri Georgia1ORCID

Affiliation:

1. Diabetes Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy

2. Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY

3. Tissue Analysis Core, Immunology Laboratory, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD

4. San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy

5. Pediatric Immunohematology and Bone Marrow Transplantation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy

6. Vita-Salute San Raffaele University, Milan, Italy

7. Department of Pathology, Immunology, and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL

8. Department of Internal Medicine, IRCCS San Raffaele Hospital, Milan, Italy

9. TrialNet Clinical Center, IRCCS San Raffaele Hospital, Milan, Italy

10. Department of Pediatrics, College of Medicine, University of Florida, Gainesville, FL

Abstract

In the attempt to understand the origin of autoantibody (AAb) production in patients with and at risk for type 1 diabetes (T1D), multiple studies have analyzed and reported alterations in T follicular helper (Tfh) cells in presymptomatic AAb+ subjects and patients with T1D. Yet, whether the regulatory counterpart of Tfh cells, represented by T follicular regulatory (Tfr) cells, is similarly altered is still unclear. To address this question, we performed analyses in peripheral blood, spleen, and pancreatic lymph nodes (PLN) of organ donor subjects with T1D. Blood analyses were also performed in living AAb− and AAb+ subjects. While negligible differences in the frequency and phenotype of blood Tfr cells were observed among T1D, AAb−, and AAb+ adult subjects, the frequency of Tfr cells was significantly reduced in spleen and PLN of T1D as compared with nondiabetic control subjects. Furthermore, adoptive transfer of Tfr cells delayed disease development in a mouse model of T1D, a finding that could indicate that Tfr cells play an important role in peripheral tolerance and regulation of autoreactive Tfh cells. Together, our findings provide evidence of Tfr cell alterations within disease-relevant tissues in patients with T1D, suggesting a role for Tfr cells in defective humoral tolerance and disease pathogenesis.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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