Treatment with Tumor Necrosis Factor-α Inhibitors, History of Allergy, and Hypercalcemia Are Risk Factors of Immune Reconstitution Inflammatory Syndrome in HIV-Negative Pulmonary Tuberculosis Patients.

IRIS TNF-α inhibitor TNFI Th1 Th2 history of allergy hypercalcemia immune reconstitution inflammatory syndrome paradoxical response tuberculosis

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
30 Dec 2019
Historique:
received: 28 11 2019
accepted: 27 12 2019
entrez: 8 1 2020
pubmed: 8 1 2020
medline: 8 1 2020
Statut: epublish

Résumé

Immune reconstitution inflammatory syndrome (IRIS) is an immune reaction that occurs along with the recovery of the patient's immunity. Tuberculosis-related IRIS (TB-IRIS) upon tumor necrosis factor (TNF)-α inhibitor treatment has been reported in non-human immunodeficiency virus (HIV) patients. However, the importance of biological treatment, as a risk factor of IRIS, has not yet been established. In this study, we examined TB-IRIS in non-HIV patients to explore the role of TNF-α inhibitor treatment. Out of 188 patients with pulmonary TB, seven patients had IRIS. We examined univariate logistic and multivariate analysis to elucidate risk factors of TB-IRIS. Univariate analysis indicated that usage of immunosuppressive drugs, TNF-α inhibitors, and history of food or drug allergy were significantly related with TB-IRIS. On initial treatment, the values of serological markers such as serum albumin and serum calcium were significantly related with TB-IRIS. There was a higher mortality rate in patients with TB-IRIS. Furthermore, multivariate analysis revealed that usage of TNF-α inhibitors, history of allergy, and serum hypercalcemia were related to TB-IRIS. Usage of TNF-α inhibitors, history of allergy, and serum hypercalcemia may be independent predictors of TB-IRIS in non-HIV patients. Since higher mortality has been reported for TB-IRIS, we should pay attention to TB patients with these risk factors.

Identifiants

pubmed: 31905985
pii: jcm9010096
doi: 10.3390/jcm9010096
pmc: PMC7019635
pii:
doi:

Types de publication

Journal Article

Langues

eng

Déclaration de conflit d'intérêts

None declared.

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Auteurs

Yoshimasa Hachisu (Y)

Department of Allergy and Respiratory Medicine, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.
Maebashi Red Cross Hospital, Gunma 371-0813, Japan.

Yasuhiko Koga (Y)

Department of Allergy and Respiratory Medicine, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.

Shu Kasama (S)

Institute for Clinical and Translational Science, Nara Medical University Hospital, Nara 634-8522, Japan.

Kyoichi Kaira (K)

Department of Respiratory Medicine, Comprehensive Cancer Center, International Medical Center, Saitama Medical University, Saitama 350-1298, Japan.

Masakiyo Yatomi (M)

Department of Allergy and Respiratory Medicine, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.

Haruka Aoki-Saito (H)

Department of Allergy and Respiratory Medicine, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.

Hiroaki Tsurumaki (H)

Department of Allergy and Respiratory Medicine, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.

Yosuke Kamide (Y)

Clinical Research Center for Allergy and Rheumatology. Sagamihara National Hospital, Kanagawa 252-0392, Japan.

Noriaki Sunaga (N)

Department of Allergy and Respiratory Medicine, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.

Toshitaka Maeno (T)

Department of Allergy and Respiratory Medicine, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.

Tamotsu Ishizuka (T)

Third Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui 910-1193, Japan.

Takeshi Hisada (T)

Gunma University Graduate School of Health Sciences, Gunma 371-8514, Japan.

Classifications MeSH