[Anti-Jo1 antibodies syndrome in an HIV-infected patient].

Ann Med Interne (Paris)

Unité de Maladies Infectieuses et Tropicales, Centre Hospitalier Universitaire Paul-Brousse, 14, avenue Paul-Vaillant-Couturier, BP 200, 94804 Villejuif Cedex, France.

Published: May 2002

An HIV-infected man developed primary polymyositis (fever, myalgia, elevated serum muscle enzymes, and signs of inflammation) associated with serum anti-Jo1 antibodies and pulmonary fibrosis. Anti-Jo1 antibodies are exceptional in HIV-infected patients. We discuss the role of infection in polymyositis. HAART and corticosteroids led to rapid clinical and radiological improvement.

Download full-text PDF

Source

Publication Analysis

Top Keywords

anti-jo1 antibodies
8
[anti-jo1 antibodies
4
antibodies syndrome
4
syndrome hiv-infected
4
hiv-infected patient]
4
patient] hiv-infected
4
hiv-infected man
4
man developed
4
developed primary
4
primary polymyositis
4

Similar Publications

Pulmonary manifestations of the idiopathic inflammatory myopathies in a South African population.

Afr J Thorac Crit Care Med

October 2024

Department of Medicine, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Article Synopsis
  • Pulmonary complications are a significant health issue for patients with idiopathic inflammatory myopathies (IIMs) in South Africa, causing high morbidity and mortality rates.
  • A study reviewed clinical records of adult IIM patients with respiratory issues in a tertiary care facility, revealing that most patients suffered from dermatomyositis and exhibited symptoms like dyspnoea and dry cough.
  • Interstitial lung disease (ILD) emerged as the most common complication, with associations found between respiratory symptoms and poorer lung function outcomes over time.
View Article and Find Full Text PDF

[Clinical associations of anti-Jo1 antibodies in a Moroccan population].

Ann Biol Clin (Paris)

November 2024

Laboratoire d'Immunologie, Centre de Recherche Clinique, CHU Mohammed VI, Marrakech, Maroc, Laboratoire de Recherche en Biosciences, Faculté de Médecine et de Pharmacie, Université Cadi Ayyad, Marrakech, Maroc.

Anti-Jo1 antibodies are usually known markers of myositis. However, they can be associated with different pathologies. We aimed to determine the immuno-clinical characteristics of patients with positive anti-Jo1.

View Article and Find Full Text PDF

273rd ENMC International workshop: Clinico-Sero-morphological classification of the Antisynthetase syndrome. Amsterdam, The Netherlands, 27-29 October 2023.

Neuromuscul Disord

December 2024

Sorbonne Université, Assistance Publique Hôpitaux de Paris, National Reference Center for Inflammatory Myopathies, Pitié-Salpêtrière Hospital, 85 Bd de l'Hôpital, 75013 Paris, France.

Article Synopsis
  • Antisynthetase syndrome is a subtype of idiopathic inflammatory myopathies, characterized by symptoms like muscle inflammation, lung issues, arthritis, rashes, and fever.
  • Muscle biopsies reveal unique morphological features that help differentiate Antisynthetase syndrome from other myositis types.
  • The workshop aims to establish a consensus on the syndrome's definition, discuss clinical and laboratory profiles, and provide management strategies and classification criteria.
View Article and Find Full Text PDF

Myositis-Associated Interstitial Lung Disease: The Experience of a Tertiary Center.

J Clin Med

October 2024

Rheumatology Department, Unidade Local de Saúde Santa Maria (ULSSM), 1649-028 Lisbon, Portugal.

: Interstitial lung disease (ILD) is a common extra-muscular manifestation of idiopathic inflammatory myopathies (IIMs), often associated with a poorer prognosis and increased mortality risk. : This retrospective study aimed to characterize lung involvement and treatment response in an IIM cohort at a Portuguese tertiary center, followed between June 2016 and March 2024. We analyzed data from high-resolution computed tomography (HRCT) scans and pulmonary function tests (PFTs) to assess associations with autoantibody profiles and treatment regimens.

View Article and Find Full Text PDF
Article Synopsis
  • * A total of 69 patients were analyzed, showing high concordance for certain antibodies (like anti-Ku and anti-PM/Scl) and moderate agreement for others (like anti-Jo1 and anti-Mi-2), while some antibodies could only be detected by one method.
  • * The results suggest that LB may be more sensitive for detecting multiple MSAs and specific antibodies, while IP performs well for dermatomyositis-associated MSAs
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!