Case Reports in Immunology

Case Reports in Immunology / 2019 / Article

Case Report | Open Access

Volume 2019 |Article ID 8746249 | 3 pages | https://doi.org/10.1155/2019/8746249

Primary Immunodeficiency with Severe Multi-Organ Immune Dysregulation

Academic Editor: Elena Bozzola
Received21 Aug 2019
Revised05 Nov 2019
Accepted12 Nov 2019
Published28 Dec 2019

Abstract

Polyglandular autoimmune syndrome type 1, also known as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), is a rare primary immunodeficiency disorder with multi-organ involvement. Besides for being predisposed to severe life-threatening infections, patients with APECED are also prone to organ impairment secondary to severe autoimmunity. As this is an autosomal recessive disorder, a biallelic mutation in the AIRE gene is responsible for APECED. The author presents a case of APECED with a single AIRE mutation. Whole exome sequencing identified a mutation in the BTNL2 gene that the author suggests may have contributed to the patient’s presentation.

1. Background

Polyglandular autoimmune syndrome type 1, also known as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) syndrome, is a rare autosomal recessive disorder that presents with multi-organ involvement. Autoimmune disease is a hallmark of this disorder and its genetic etiology is a biallelic mutation in the AIRE gene that is responsible for immune regulation. The author presents a case of a patient with clinical APECED and a single pathogenic AIRE mutation. Whole exome sequencing identified a mutation in the BTNL2 gene that codes for the butyrophilin-like 2 (MHC class II associated) protein and one that the author proposes may have contributed to his disease.

2. Case Description

A 15-year-old male patient presented with multiple autoimmune polyendocrinopathies (Tables 1 and 2). He had adrenal insufficiency, hypothyroidism, and hypoparathyroidism. He also had gluten-sensitive enteropathy and pancreatic insufficiency. The development of autoimmune hepatitis necessitated the initiation of systemic corticosteroids with a transition to oral tacrolimus 2 mg daily. The patient developed severe gastroparesis that required a gastrostomy-jejunostomy (G-J) tube in order to maintain appropriate nutritional support. He had recurrent nasal polyposis as well as one episode of an aural polyp in his left middle ear canal that required surgical resection. The patient developed Sjogren’s syndrome, vitiligo, and candidal onychomycosis. He had recurrent infectious sinusitis and otitis, as well as more than ten episodes of pneumonia that required treatment with systemic antibiotics.


ConditionAge

Oral thrush9 months
Pancreatic insufficiency2 years
Adrenal insufficiency3
Uveitis4
Candidal onychomycosis5
Enteropathy6
Alopecia7
Raynaud’s disease7
Vitiligo8
Sjogren’s syndrome10
Hypoparathyroidism11
Hypothyroidism12
Gastroparesis12
Nasal polyps, recurrent12
Aural polyp12
Megacolon12
Autoimmune hepatitis15


Antibody (units)ResultsReference Range

ANAnegativenegative
DsDNA (IU/mL)1.1<70.1
Rheumatoid factor (IU/mL)<9.90–22
Thyroglobulin (ng/mL)00
Anti-TPO antibody (IU/mL)567.20–5
Glutamic acid decarboxylase antibody (IU/mL)>250<5

His mother is of Italian and Finnish heritage. His father is of Castilian descent. While his father is healthy, his mother has periodic fever syndrome, rheumatoid arthritis, Raynaud’s disease, and hypoparathyroidism. The patient has one sibling, an older brother who has Raynaud’s disease.

Flow cytometry quantified normal lymphocyte subpopulations (Table 3). Lymphocyte proliferation on mitogenic stimulation to PHA, ConA, and Pokeweed were within normal limits, as were antigenic responses to tetanus and candida. At the time of his evaluation he was already on immunoglobulin replacement therapy and his pretreatment immunoglobulin levels were not available. CD4+CD25+CD127low populations were within normal limits making immunodysregulation polyendocrinopathy enteropathy X-linked (IPEX) unlikely. The clinical presentation was most consistent with APECED and genetic testing was therefore obtained.


LymphocytePercentageCells/µL

T+B+NK+792170
CD4+ T cells461251
CD8+ T cells26720
CD19+ B cells11320
CD16+CD56+ NK cells6180

Genetic sequencing identified a monoallelic pathogenic variant p.Arg257Ter in the AIRE gene at the c.769 C>T coding DNA. Further sequencing identified an exonic monoallelic frameshift mutation in the BTNL2 gene at the enhancer coding sequence region 6:32370969 (TG>T), rs139418003 coding for p.His151ThrfsTer96.

3. Discussion

This case demonstrates a clinical phenotype of APECED but with a monoallelic pathogenic AIRE mutation. Further sequencing was therefore obtained in order to identify another possible contributing genetic factor.

The thymus is the site of T cell development and where central tolerance occurs. This organ is divided into the cortex and medulla, of which thymic epithelial cells (TECs) are a major component. The autoimmune regulator (AIRE) gene is critical for the development of the central T cell tolerance [1]. AIRE is a transcription regulator that is primarily expressed in the medullary thymic epithelial cells (mTECs), although its expression has also been identified in other peripheral organs such as the pancreas, testes, appendix, and adrenal cortex [2, 3]. mTECs express tissue-specific genes and tissue-restricted antigens (TRAs) that are presented to T cells within the context of major histocompatibility complexes (MHCs). AIRE regulates the expression of these tissue-specific genes and TRAs [3, 4]. High affinity T-cell receptor (TCR) interactions with MHC-presented self-antigens in the thymic tissue either induce the deletion of thymocytes by apoptosis or shift the T cells into regulatory T cell (Treg) development, thereby preventing autoimmunity [5, 6].

The severe autoimmunity that is seen in APECED is a result of defective AIRE function [7]. More than 100 mutations in the AIRE gene have been identified in autoimmune diseases. AntiIL17 autoantibody production, a cytokine that is important for antifungal immunity, has been identified in APECED. AIRE is also required for the function of the antifungal responses of Dectin-1 and Dectin-2 receptors [8]. These defects explain the predisposition of patients with APECED to developing candidiasis [9].

BTNL2 is a butyrophilin family member with homology to the B7 costimulatory molecules. Although its full immunoregulatory capacity has not yet been fully described, BTNL2 serves as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release [1012]. BTNL2 prevents B7-ICOS costimulation and downregulates T cell activation in vitro. Mouse studies have shown that recombinant mouse BTNL2 modifies B7/CD28 signaling to promote expression of Foxp3, a transcription factor involved in regulatory T cell development [13].

BTNL2 is highly expressed in lymphoid tissue. It has been localized to Peyer’s patches of the small intestine as well as epithelial and dendritic cells within gastrointestinal tissue. Altered expression of BTNL2 is associated with inflammatory bowel disease [14]. Mutations in this gene are further associated with other autoimmune conditions including sarcoidosis, rheumatoid arthritis, vitiligo, and psoriasis [1518]. BTNL2 has also been implicated in autoimmune thyroid disease [19, 20].

Given the location of the presently identified BTNL2 frameshift mutation and its role in the regulation of T cell-mediated responses, the author proposes that this mutation may have contributed to the development of the severe autoimmune manifestations in this patient with a single pathogenic AIRE mutation. Continued reports of genetic polymorphisms of the BTNL2 gene in the presence of autoimmunity will allow for a better understanding of the scope of this gene’s impact on immunoregulatory pathways.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

The author thanks the Jeffrey Modell Foundation for its grant support of the work presented in this manuscript.

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Copyright © 2019 Tatyana Gavrilova. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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