Autoimmune and/or Inflammatory Diseases and Cancers: A Multifaceted Association

A special issue of Journal of Clinical Medicine (ISSN 2077-0383). This special issue belongs to the section "Immunology".

Deadline for manuscript submissions: closed (15 December 2022) | Viewed by 3821

Special Issue Editor


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Guest Editor
Department of Internal Medicine - Multi-Organic Diseases, Saint Eloi Hospital – Montpellier -1 University, 80 Avenue Augsutin Fliche, CEDEX 5, 34295 Montpellier, France
Interests: systemic sclerosis/scleroderma; lupus; Sjögren’s syndrome; inflammatory myopathies; vasculitides; anti-neutrophil cytoplasmic antibodies; giant cell arteritis; Still’s disease; Behcet’s disease; immune deficiency; stem cell therapy; mesenchymal stem cells; immunotherapy of cancer

Special Issue Information

Dear Colleagues,

Autoimmune and/or inflammatory diseases (AIID) include non-organ-specific systemic autoimmune diseases, including connective tissue disorders (such as rheumatoid arthritis, systemic lupus, Sjögren’s syndrome, systemic sclerosis, and inflammatory myopathies) and vasculitides (such as ANCA-associated vasculitides, cryoglobulinemia, IgA vasculitis, periarteritis nodosa, giant cell arteritis, etc.). Several other diseases are limited to one single organ through autoimmunity (organ-specific autoimmune diseases such as Hashimoto thyroiditis) or inflammation (such as inflammatory bowel diseases). We have to also mention the group of autoinflammatory diseases which have recently been enriched with a new entity called VEXAS.

While the relationships between AIID and cancers (solid and/or hematological) have been studied now for several decades, recent years are marked by an increasing amount of robust scientific data and researches concerning this association. For example, the association between systemic sclerosis and cancer is now well documented, while myelodysplastic syndromes are now considered as conditions favoring inflammatory diseases. Therefore, recent years have been very exciting and promising, reinforced by the emerging interest regarding the role of the immune system against cancer. Furthermore, immune checkpoint inhibitors are powerful therapeutic weapons against cancer, but they may also induce autoimmune adverse events, close to classical AIID. Therefore, the association between AIID and cancer may appear as a double-edged sword, and the concept of autoimmune paraneoplastic syndrome is emerging in several fields (notable, neurological, and systemic diseases).

This topic aims to outline the association between AIID and cancers (epidemiology, clinical characteristics, pathophysiological mechanisms, and therapeutic features).

Welcome to all relevant articles, including research articles, review articles as well as short communications.

Prof. Dr. Philippe Guilpain
Guest Editor

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Keywords

  • connective tissue disorders
  • lupus
  • Sjögren’s syndrome
  • inflammatory myopathy
  • systemic sclerosis
  • vasculitides
  •  rheumatoid arthritis
  • ANCA-associated vasculitides
  • periarteritis nodosa
  • IgA vasculitis
  • Giant cell arteritis
  • VEXAS
  • autoinflammatory diseases
  • organ specific autoimmune diseases
  • thyroiditis
  • myasthenia gravis
  • inflammatory bowel diseases
  • paraneoplastic syndromes
  • solid cancers
  • hematological cancers
  • myelodysplastic syndromes

Published Papers (2 papers)

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13 pages, 4007 KiB  
Article
Incidence of Gastric Neoplasms Arising from Autoimmune Metaplastic Atrophic Gastritis: A Systematic Review and Case Reports
by Chuyan Chen, Yi Yang, Peng Li and Haiyi Hu
J. Clin. Med. 2023, 12(3), 1062; https://doi.org/10.3390/jcm12031062 - 30 Jan 2023
Cited by 7 | Viewed by 2242
Abstract
Autoimmune metaplastic atrophic gastritis (AMAG) is associated with an increased risk of gastric neoplasms. This study aimed to systematically analyze the incidence rate of gastric cancer (GC), low-grade dysplasia (LGD) and type-1 gastric neuroendocrine tumor (gNETs) development in AMAG adults. Studies on AMAG [...] Read more.
Autoimmune metaplastic atrophic gastritis (AMAG) is associated with an increased risk of gastric neoplasms. This study aimed to systematically analyze the incidence rate of gastric cancer (GC), low-grade dysplasia (LGD) and type-1 gastric neuroendocrine tumor (gNETs) development in AMAG adults. Studies on AMAG patients reporting the incidence of gastric neoplasms was identified through a systematic search in PUBMED and EMBASE. Study quality was assessed using the Joanna Briggs Institute quality assessment tool. Incidence rates of GC, LGD and type-1 gNETs were examined by meta-analysis. Thirteen studies met eligibility criteria. Incidence rate of gastric cancer calculated from the pooled data was 0.14% per person-year in both single-center studies and national registration studies. Meta-analysis showed a relative risk of 11.05 (95% CI: 6.39–19.11) for gastric cancer development in AMAG patients. The calculated pooled gastric LGD and type-1 gNETs incidence rates were 0.52% and 0.83% per person-year, respectively. As for experience from our center, we presented three distinctive cases of gastric neoplasm arising from the background of AMAG. This study underscores the potential for malignant transformation of precancerous lesions and reiterates the importance of careful esophagogastroduodenoscopy screening. Full article
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9 pages, 11096 KiB  
Case Report
Comparison of Clinical Manifestations and Pathology between Kimura Disease and IgG4-Related Disease: A Report of Two Cases and Literature Review
by Sing-Ya Chang, Chih-Chun Lee, Ming-Ling Chang, Wen-Chieh Teng, Chao-Yang Hsiao, Han-Hua Yu, Meng-Ju Hsieh and Tien-Ming Chan
J. Clin. Med. 2022, 11(23), 6887; https://doi.org/10.3390/jcm11236887 - 22 Nov 2022
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Abstract
Kimura disease (KD) is a rare, chronic proliferative condition presenting as a subcutaneous mass predominantly located in the head and neck region; it is characterized by eosinophilia and elevated serum IgE levels. IgG4-related disease (IgG4RD) is a fibroinflammatory condition characterized by swelling in [...] Read more.
Kimura disease (KD) is a rare, chronic proliferative condition presenting as a subcutaneous mass predominantly located in the head and neck region; it is characterized by eosinophilia and elevated serum IgE levels. IgG4-related disease (IgG4RD) is a fibroinflammatory condition characterized by swelling in single or multiple organs and the infiltration of IgG4 plasma cells. Herein, we presented two cases. Case 1 is a 38-year-old man with a painless mass in his right postauricular region, and Case 2 is a 36-year-old man with painless lymphadenopathy in his bilateral postauricular region. After surgical excision, they showed good recovery with no relapse. Although Cases 1 and 2 shared several overlapping pathological manifestations, there were a few differences that allowed the differentiation of KD and IgG4RD. Full article
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