Abstract

In this study, the clinical and immunogenetical features in a cohort of Chinese patients with BCGosis/BCGitis were investigated. For the patients with abnormal immunological functions, Sanger sequencing was used to identify the involved genes. There were 74 confirmed cases of BCGosis/BCGitis during 2007–2012. Classified by infected tissues and organs, no cases only had local infection, 39 patients had a regional infection, 21 patients had a distant infection and 14 patients had a disseminated infection. Thirty-two patients (43.2%) had definitive primary immunodeficiency diseases (PID) and chronic granulomatous disease (CGD) is the most common PID (n = 23, accounted for 71.9% of all PID patients). For CGD patients, based on the anti-tuberculosis treatment, administration of rhIFN-γ resulted in better control of BCGosis/BCGitis. The results indicate that PIDs are associated with susceptibility to BCG disease. For children with BCGosis/BCGitis, immune function evaluation is necessary, and IFN-γ treatment for BCGosis/BCGitis patients with CGD is effective.

Highlights

  • The Bacillus Calmette-Guerin (BCG) vaccine has existed for 80 years and is one of the most widely used of all current vaccines

  • There is no significant difference in the age of onset of BCGosis/BCGitis between these two groups

  • The BCG vaccine has existed for 80 years and is one of the most widely used of all current vaccines, reaching .80% of neonates and infants in countries where it is part of the national childhood immunization program [1]

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Summary

Introduction

The Bacillus Calmette-Guerin (BCG) vaccine has existed for 80 years and is one of the most widely used of all current vaccines. The BCG vaccine has a protective effect against meningitis and disseminated tuberculosis (TB) in children [1]. The World Health Organization (WHO) recommends that all infants in highly endemic countries receive a single dose of the BCG vaccine [2]. The incidence of BCG infection is approximately 1:10,000–1:1,000,000 [3]. The BCG-induced disease phenotypes were designated as local, regional, distant, or disseminated pattern based on a revised pediatric classification proposed by Hesseling et al [4]. The former two patterns were conventionally termed as BCGitis and the latter two as BCGosis

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