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1381. M.genavense in the ART Era: From Persistent Disseminated Disease to Severe Disease

BACKGROUND: Mycobacterium genavense is an opportunistic pathogen in HIV patients that is difficult to culture and difficult to manage clinically. Here we describe three cases of HIV patients with Mycobacterium genavense with courses representing the spectrum of M.genavense presentations in the curre...

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Autores principales: Manion, Maura, Lynn, Niamh, Pei, Luxin, Hammoud, Dima, Laidlaw, Elizabeth, Roby, Gregg, Metzger, Dorinda, Mejia, Yolanda, Lisco, Andrea, Bergin, Colm, Sereti, Irini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6809023/
http://dx.doi.org/10.1093/ofid/ofz360.1245
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author Manion, Maura
Lynn, Niamh
Pei, Luxin
Hammoud, Dima
Laidlaw, Elizabeth
Roby, Gregg
Metzger, Dorinda
Mejia, Yolanda
Lisco, Andrea
Bergin, Colm
Sereti, Irini
author_facet Manion, Maura
Lynn, Niamh
Pei, Luxin
Hammoud, Dima
Laidlaw, Elizabeth
Roby, Gregg
Metzger, Dorinda
Mejia, Yolanda
Lisco, Andrea
Bergin, Colm
Sereti, Irini
author_sort Manion, Maura
collection PubMed
description BACKGROUND: Mycobacterium genavense is an opportunistic pathogen in HIV patients that is difficult to culture and difficult to manage clinically. Here we describe three cases of HIV patients with Mycobacterium genavense with courses representing the spectrum of M.genavense presentations in the current ART era complicated by differing divergent immune responses. METHODS: Two patients were in a longitudinal study at NIAID enrolling patients with HIV and suspected IRIS (PANDORA) (NCT02147405) and one was seen at St. James’s hospital in Dublin. Frozen peripheral blood mononuclear cells were collected at the time of presentation and were used for in vitro stimulation with irradiated M. genavenese in cases 1 and 2 to detect production of cytokines by CD4 T cells. RESULTS: Pt 1: 27-year old male with M. genavense presenting as diarrhea, abdominal pain, skin nodules, hepatosplenomegaly, and lymphadenopathy (LAN) that persisted on one year of anti-mycobacterial therapy and ART. No CD4 T-cell cytokine response to M. genevense genavense was detected (Fig 1). He received interferon-g and optimization of his antimycobacterial regimen with improvement of symptoms and decreased pathogen burden on repeated biopsies. Pt 2: 55-year old female with M. genavense IRIS manifesting as fevers and abdominal pain that persisted for 10 months on ART (CD4 109 cells/µmL) requiring intermittent corticosteroid use complicated by adrenal insufficiency. She had evidence of CD4 T-cell response to M. genavense in vitro and improved with optimization of her anti-mycobacterial and corticosteroid regimen. Pt 3: 39-year-old male with M. genavense IRIS presenting as fevers, LAN, pleuritic chest pain, and abdominal pain on ART (CD4 19 c/mµL) persisting despite immunologic response to ARV therapy (CD4 recovery to 419 c/mL), appropriate anti-mycobacterial therapy and corticosteroids. He required 4 doses of infliximab (5 mg/kg IV) that facilitated tapering of prednisone. CONCLUSION: The clinical presentation of Mycobacterium genavense in HIV patients in the ARV era range from disseminated disease with poor immune reconstitution to persistent or severe IRIS requiring immune suppression. Effective clinical outcomes relied on appropriate anti-mycobacterial and either immune-boosting or immune-suppressive therapies. [Image: see text] DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68090232019-10-28 1381. M.genavense in the ART Era: From Persistent Disseminated Disease to Severe Disease Manion, Maura Lynn, Niamh Pei, Luxin Hammoud, Dima Laidlaw, Elizabeth Roby, Gregg Metzger, Dorinda Mejia, Yolanda Lisco, Andrea Bergin, Colm Sereti, Irini Open Forum Infect Dis Abstracts BACKGROUND: Mycobacterium genavense is an opportunistic pathogen in HIV patients that is difficult to culture and difficult to manage clinically. Here we describe three cases of HIV patients with Mycobacterium genavense with courses representing the spectrum of M.genavense presentations in the current ART era complicated by differing divergent immune responses. METHODS: Two patients were in a longitudinal study at NIAID enrolling patients with HIV and suspected IRIS (PANDORA) (NCT02147405) and one was seen at St. James’s hospital in Dublin. Frozen peripheral blood mononuclear cells were collected at the time of presentation and were used for in vitro stimulation with irradiated M. genavenese in cases 1 and 2 to detect production of cytokines by CD4 T cells. RESULTS: Pt 1: 27-year old male with M. genavense presenting as diarrhea, abdominal pain, skin nodules, hepatosplenomegaly, and lymphadenopathy (LAN) that persisted on one year of anti-mycobacterial therapy and ART. No CD4 T-cell cytokine response to M. genevense genavense was detected (Fig 1). He received interferon-g and optimization of his antimycobacterial regimen with improvement of symptoms and decreased pathogen burden on repeated biopsies. Pt 2: 55-year old female with M. genavense IRIS manifesting as fevers and abdominal pain that persisted for 10 months on ART (CD4 109 cells/µmL) requiring intermittent corticosteroid use complicated by adrenal insufficiency. She had evidence of CD4 T-cell response to M. genavense in vitro and improved with optimization of her anti-mycobacterial and corticosteroid regimen. Pt 3: 39-year-old male with M. genavense IRIS presenting as fevers, LAN, pleuritic chest pain, and abdominal pain on ART (CD4 19 c/mµL) persisting despite immunologic response to ARV therapy (CD4 recovery to 419 c/mL), appropriate anti-mycobacterial therapy and corticosteroids. He required 4 doses of infliximab (5 mg/kg IV) that facilitated tapering of prednisone. CONCLUSION: The clinical presentation of Mycobacterium genavense in HIV patients in the ARV era range from disseminated disease with poor immune reconstitution to persistent or severe IRIS requiring immune suppression. Effective clinical outcomes relied on appropriate anti-mycobacterial and either immune-boosting or immune-suppressive therapies. [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6809023/ http://dx.doi.org/10.1093/ofid/ofz360.1245 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Manion, Maura
Lynn, Niamh
Pei, Luxin
Hammoud, Dima
Laidlaw, Elizabeth
Roby, Gregg
Metzger, Dorinda
Mejia, Yolanda
Lisco, Andrea
Bergin, Colm
Sereti, Irini
1381. M.genavense in the ART Era: From Persistent Disseminated Disease to Severe Disease
title 1381. M.genavense in the ART Era: From Persistent Disseminated Disease to Severe Disease
title_full 1381. M.genavense in the ART Era: From Persistent Disseminated Disease to Severe Disease
title_fullStr 1381. M.genavense in the ART Era: From Persistent Disseminated Disease to Severe Disease
title_full_unstemmed 1381. M.genavense in the ART Era: From Persistent Disseminated Disease to Severe Disease
title_short 1381. M.genavense in the ART Era: From Persistent Disseminated Disease to Severe Disease
title_sort 1381. m.genavense in the art era: from persistent disseminated disease to severe disease
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6809023/
http://dx.doi.org/10.1093/ofid/ofz360.1245
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