Biliary cirrhosis in a child with inherited interleukin-12 deficiency.
Interleukin-12 (IL-12) is a key cytokine in the defense against intracellular bacteria notably Mycobacteria and Salmonella species. We report a case of disseminated mycobacterial infection, following BCG vaccination, in a child who later developed tuberculosis. Functional tests and a novel diagnosti...
Main Authors: | , , , , , , , , , , |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2008
|
_version_ | 1797092050422726656 |
---|---|
author | Pulickal, A Hambleton, S Callaghan, M Moore, C Goulding, J Goodsall, A Baretto, R Lammas, D Anderson, S Levin, M Pollard, A |
author_facet | Pulickal, A Hambleton, S Callaghan, M Moore, C Goulding, J Goodsall, A Baretto, R Lammas, D Anderson, S Levin, M Pollard, A |
author_sort | Pulickal, A |
collection | OXFORD |
description | Interleukin-12 (IL-12) is a key cytokine in the defense against intracellular bacteria notably Mycobacteria and Salmonella species. We report a case of disseminated mycobacterial infection, following BCG vaccination, in a child who later developed tuberculosis. Functional tests and a novel diagnostic polymerase chain reaction (PCR) assay, revealed a loss-of-function deletion in the IL12 gene. Analysis of samples from the parents and siblings of the patient indicated an autosomal recessive inheritance pattern with varying degrees of phenotypic expression in identical genotypes. Interferon-gamma (IFN-gamma) therapy was associated with marked clinical improvement. Biliary cirrhosis, a hitherto unreported complication of IL-12 deficiency, developed later and required liver transplantation. A defect in the IL-12-IFN-gamma pathway should be suspected in patients presenting with multiple, repeated or persistent infection with intracellular bacteria. The diagnostic work-up and the immuno-genetic assay described here can aid in the quick and reliable diagnosis of IL-12 deficiency resulting from genetic defects and its subsequent management. |
first_indexed | 2024-03-07T03:40:48Z |
format | Journal article |
id | oxford-uuid:bdd29a69-197e-4d25-a036-479fedf87e48 |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T03:40:48Z |
publishDate | 2008 |
record_format | dspace |
spelling | oxford-uuid:bdd29a69-197e-4d25-a036-479fedf87e482022-03-27T05:34:41ZBiliary cirrhosis in a child with inherited interleukin-12 deficiency.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:bdd29a69-197e-4d25-a036-479fedf87e48EnglishSymplectic Elements at Oxford2008Pulickal, AHambleton, SCallaghan, MMoore, CGoulding, JGoodsall, ABaretto, RLammas, DAnderson, SLevin, MPollard, AInterleukin-12 (IL-12) is a key cytokine in the defense against intracellular bacteria notably Mycobacteria and Salmonella species. We report a case of disseminated mycobacterial infection, following BCG vaccination, in a child who later developed tuberculosis. Functional tests and a novel diagnostic polymerase chain reaction (PCR) assay, revealed a loss-of-function deletion in the IL12 gene. Analysis of samples from the parents and siblings of the patient indicated an autosomal recessive inheritance pattern with varying degrees of phenotypic expression in identical genotypes. Interferon-gamma (IFN-gamma) therapy was associated with marked clinical improvement. Biliary cirrhosis, a hitherto unreported complication of IL-12 deficiency, developed later and required liver transplantation. A defect in the IL-12-IFN-gamma pathway should be suspected in patients presenting with multiple, repeated or persistent infection with intracellular bacteria. The diagnostic work-up and the immuno-genetic assay described here can aid in the quick and reliable diagnosis of IL-12 deficiency resulting from genetic defects and its subsequent management. |
spellingShingle | Pulickal, A Hambleton, S Callaghan, M Moore, C Goulding, J Goodsall, A Baretto, R Lammas, D Anderson, S Levin, M Pollard, A Biliary cirrhosis in a child with inherited interleukin-12 deficiency. |
title | Biliary cirrhosis in a child with inherited interleukin-12 deficiency. |
title_full | Biliary cirrhosis in a child with inherited interleukin-12 deficiency. |
title_fullStr | Biliary cirrhosis in a child with inherited interleukin-12 deficiency. |
title_full_unstemmed | Biliary cirrhosis in a child with inherited interleukin-12 deficiency. |
title_short | Biliary cirrhosis in a child with inherited interleukin-12 deficiency. |
title_sort | biliary cirrhosis in a child with inherited interleukin 12 deficiency |
work_keys_str_mv | AT pulickala biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT hambletons biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT callaghanm biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT moorec biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT gouldingj biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT goodsalla biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT barettor biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT lammasd biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT andersons biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT levinm biliarycirrhosisinachildwithinheritedinterleukin12deficiency AT pollarda biliarycirrhosisinachildwithinheritedinterleukin12deficiency |