Frontiers in Immunology (Jan 2022)
Phenomic Analysis of Chronic Granulomatous Disease Reveals More Severe Integumentary Infections in X-Linked Compared With Autosomal Recessive Chronic Granulomatous Disease
- Timothy Lok-Hin Chiu,
- Daniel Leung,
- Koon-Wing Chan,
- Hok Man Yeung,
- Chung-Yin Wong,
- Huawei Mao,
- Jianxin He,
- Pandiarajan Vignesh,
- Weiling Liang,
- Woei Kang Liew,
- Li-Ping Jiang,
- Tong-Xin Chen,
- Xiang-Yuan Chen,
- Yin-Bo Tao,
- Yong-Bin Xu,
- Hsin-Hui Yu,
- Alta Terblanche,
- David Christopher Lung,
- Cheng-Rong Li,
- Jing Chen,
- Man Tian,
- Brian Eley,
- Xingtian Yang,
- Jing Yang,
- Wen Chin Chiang,
- Bee Wah Lee,
- Bee Wah Lee,
- Deepti Suri,
- Amit Rawat,
- Anju Gupta,
- Surjit Singh,
- Wilfred Hing Sang Wong,
- Gilbert T. Chua,
- Jaime Sou Da Rosa Duque,
- Kai-Ning Cheong,
- Patrick Chun-Yin Chong,
- Marco Hok-Kung Ho,
- Tsz-Leung Lee,
- Wanling Yang,
- Pamela P. Lee,
- Yu Lung Lau
Affiliations
- Timothy Lok-Hin Chiu
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Daniel Leung
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Koon-Wing Chan
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Hok Man Yeung
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Chung-Yin Wong
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Huawei Mao
- Department of Immunology, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s Health, Beijing, China
- Jianxin He
- Department of Respiratory Medicine, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s Health, Beijing, China
- Pandiarajan Vignesh
- Allergy & Immunology Unit, Department of Paediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India
- Weiling Liang
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China
- Woei Kang Liew
- Paediatric Immunology Service, KK Hospital, Singapore, Singapore
- Li-Ping Jiang
- Children’s Hospital of Chongqing Medical University, Chongqing, China
- Tong-Xin Chen
- Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China
- Xiang-Yuan Chen
- Department of Allergy, Immunology and Rheumatology, Guangzhou Children’s Hospital, Guangdong, China
- Yin-Bo Tao
- Department of Allergy, Immunology and Rheumatology, Guangzhou Children’s Hospital, Guangdong, China
- Yong-Bin Xu
- 0Guangzhou Women and Children’s Medical Center, Guangzhou, China
- Hsin-Hui Yu
- 1Department of Paediatrics, National Taiwan University Children’s Hospital, Taipei, Taiwan
- Alta Terblanche
- 2Paediatric Gastroenterology and Hepatology Unit, University of Pretoria, Pretoria, South Africa
- David Christopher Lung
- 3Department of Pathology, Queen Elizabeth Hospital/Hong Kong Children’s Hospital, Hong Kong, Hong Kong SAR, China
- Cheng-Rong Li
- 4Department of Nephrology, Shenzhen Children’s Hospital, Shenzhen, China
- Jing Chen
- 5Department of Hematology/Oncology, Key Laboratory of Pediatric Hematology & Oncology Ministry of Health, Shanghai Children’s Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China
- Man Tian
- 6Department of Tuberculosis, Nanjing Chest Hospital, Nanjing, China
- Brian Eley
- 7Department of Paediatrics and Child Health, University of Cape Town and Red Cross War Memorial Children’s Hospital, Cape Town, South Africa
- Xingtian Yang
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Jing Yang
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Wen Chin Chiang
- Paediatric Immunology Service, KK Hospital, Singapore, Singapore
- Bee Wah Lee
- 8Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
- Bee Wah Lee
- 9Khoo Teck Puat-National University Children’s Medical Institute, National University Health System, Singapore, Singapore
- Deepti Suri
- Allergy & Immunology Unit, Department of Paediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India
- Amit Rawat
- Allergy & Immunology Unit, Department of Paediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India
- Anju Gupta
- Allergy & Immunology Unit, Department of Paediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India
- Surjit Singh
- Allergy & Immunology Unit, Department of Paediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India
- Wilfred Hing Sang Wong
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Gilbert T. Chua
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Jaime Sou Da Rosa Duque
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Kai-Ning Cheong
- 0Hong Kong Children’s Hospital, Hong Kong, Hong Kong SAR, China
- Patrick Chun-Yin Chong
- 1Virtus Medical, Hong Kong, Hong Kong SAR, China
- Marco Hok-Kung Ho
- 1Virtus Medical, Hong Kong, Hong Kong SAR, China
- Tsz-Leung Lee
- 0Hong Kong Children’s Hospital, Hong Kong, Hong Kong SAR, China
- Wanling Yang
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Pamela P. Lee
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- Yu Lung Lau
- Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China
- DOI
- https://doi.org/10.3389/fimmu.2021.803763
- Journal volume & issue
-
Vol. 12
Abstract
BackgroundChronic granulomatous disease (CGD) is an inborn error of immunity (IEI), characterised by recurrent bacterial and fungal infections. It is inherited either in an X-linked (XL) or autosomal recessive (AR) mode. Phenome refers to the entire set of phenotypes expressed, and its study allows us to generate new knowledge of the disease. The objective of the study is to reveal the phenomic differences between XL and AR-CGD by using Human Phenotype Ontology (HPO) terms.MethodsWe collected data on 117 patients with genetically diagnosed CGD from Asia and Africa referred to the Asian Primary Immunodeficiency Network (APID network). Only 90 patients with sufficient clinical information were included for phenomic analysis. We used HPO terms to describe all phenotypes manifested in the patients.ResultsXL-CGD patients had a lower age of onset, referral, clinical diagnosis, and genetic diagnosis compared with AR-CGD patients. The integument and central nervous system were more frequently affected in XL-CGD patients. Regarding HPO terms, perianal abscess, cutaneous abscess, and elevated hepatic transaminase were correlated with XL-CGD. A higher percentage of XL-CGD patients presented with BCGitis/BCGosis as their first manifestation. Among our CGD patients, lung was the most frequently infected organ, with gastrointestinal system and skin ranking second and third, respectively. Aspergillus species, Mycobacterium bovis, and Mycobacteirum tuberculosis were the most frequent pathogens to be found.ConclusionPhenomic analysis confirmed that XL-CGD patients have more recurrent and aggressive infections compared with AR-CGD patients. Various phenotypic differences listed out can be used as clinical handles to distinguish XL or AR-CGD based on clinical features.
Keywords
- chronic granulomatous disease (CGD)
- inborn error of immunity (IEI)
- human phenotype ontology (HPO)
- phenome
- genetics