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1.
Lung ; 179(5): 305-17, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11976898

RESUMEN

Bronchoalveolar lavage (BAL) is frequently performed in patients with suspected ocular sarcoidosis. This study describes the immunogenetical, immunological, radiological, and functional features of a subclinical alveolar lymphocytosis unrelated to sarcoidosis in patients with chronic uveitis. Two hundred and ten patients with chronic uveitis of unknown origin, who underwent fiber-optic bronchoscopy with BAL as part of a prospective protocol over a three-year period, were evaluable for retrospective analysis. Sixty-five patients had alveolar lymphocytosis: Sarcoidosis was diagnosed in 13 (6%) patients, whereas alveolar lymphocytosis was considered unrelated to sarcoidosis in 52 (25%). Alveolar lymphocytosis unrelated to sarcoidosis was not associated with radiologically detectable interstitial lung disease or pulmonary function impairment. CD4/CD8 lymphocyte ratio was 3.7 +/- 3.0. Total cell count, total lymphocyte, and CD4 lymphocyte percentage were significantly lower when compared with sarcoidosis-related alveolitis (129,000 +/- 80,000 vs. 218,000 +/- 117,000, p <0.05; 33.1% +/- 13.2 vs. 39.7% +/- 13.2, p <0.05; and 54.3% +/- 18.2 vs. 65.4% +/- 10.1, p <0.05, respectively). Patients with alveolar lymphocytosis unrelated to sarcoidosis were older (47.8 +/- 17.7 years vs. 42.7 +/- 14.2 years, p <0.05) and more likely to carry the HLA-B51 allele (19.7% vs. 7.1%, p <0.01) than patients with chronic uveitis without alveolar lymphocytosis. They did not appear to be at risk of developing clinically apparent interstitial lung disease on followup. We conclude that alveolar lymphocytosis is frequently observed in patients with chronic uveitis. It is generally unrelated to sarcoidosis and may then be associated with a distinctive immunogenetic phenotype.


Asunto(s)
Linfocitosis/complicaciones , Sarcoidosis/complicaciones , Uveítis/complicaciones , Líquido del Lavado Bronquioalveolar/citología , Broncoscopía , Relación CD4-CD8 , Enfermedad Crónica , Femenino , Humanos , Linfocitosis/inmunología , Masculino , Persona de Mediana Edad , Alveolos Pulmonares/patología , Pruebas de Función Respiratoria , Sarcoidosis/diagnóstico , Uveítis/inmunología
3.
Eur J Clin Chem Clin Biochem ; 30(6): 319-23, 1992 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-1324743

RESUMEN

In AIDS the onset of the ocular dry syndrome, characterized by lacrimal hyposecretion and deterioration of the corneal and conjunctival epithelium, generally accompanies the clinical aggravation of immunodepression. The study of serum and lacrimal proteins contributes to our knowledge of the pathophysiology of this syndrome. The lacrimal clearance of albumin indicates changes in the permeability of the haemato-lacrimal and conjunctival barrier. Lacrimal monomeric IgA and IgG are mainly of plasmatic origin, while polymeric IgA and IgM are synthesized in situ. The concentrations of these analytes thus reflect ocular humoral immune status. They show a strong humoral protein response in patients with cytomegalovirus retinitis. Lacrimal concentrations of lactoferrin and lysozyme were found to be significantly decreased in AIDS patients with ocular dryness, reflecting a decrease in the secretory activity of the lacrimal gland. Moreover, ocular lympho-plasmocyte infiltration was observed in several patients, with an increase in lacrimal beta 2-microglobulin concentrations. These various lacrimal proteins could be good markers of the ocular dry syndrome in AIDS.


Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/metabolismo , Síndromes de Ojo Seco/metabolismo , Proteínas del Ojo/metabolismo , VIH-1/metabolismo , Adulto , Proteínas Sanguíneas/metabolismo , Relación CD4-CD8 , Infecciones por Citomegalovirus/metabolismo , Infecciones Virales del Ojo/metabolismo , Proteínas del Ojo/biosíntesis , Infecciones por VIH/metabolismo , Humanos , Masculino , Permeabilidad , Retinitis/metabolismo , Retinitis/microbiología
4.
Presse Med ; 19(29): 1355-8, 1990 Sep 15.
Artículo en Francés | MEDLINE | ID: mdl-2146608

RESUMEN

Seventeen patients with Behçet's disease were treated with intermittent intravenous bolus injections of cyclophosphamide. Twelve patients had severe eye lesions, 7 had central neurological disorders and 2 had both ocular and central nervous system involvement. Cyclophosphamide was given during 4 weeks on average, in mean doses of 922 +/- 127 mg. Each patient received an average of 10 +/- 5 injections. The drug was generally well tolerated; only one patient developed moderate and transient hepatocytolysis. Visual acuity was improved in 12 of the 22 eyes with active lesions, and signs of inflammation disappeared in all cases. Neurological improvement was observed in 5 of the 7 patients affected, with complete regression of the disorders in 2 of them. In 16 patients who were also under corticosteroid therapy, steroid dosage could be significantly reduced by 44 +/- 11 mg per day.


Asunto(s)
Síndrome de Behçet/tratamiento farmacológico , Ciclofosfamida/uso terapéutico , Corticoesteroides/uso terapéutico , Adulto , Síndrome de Behçet/sangre , Síndrome de Behçet/complicaciones , Ciclofosfamida/administración & dosificación , Oftalmopatías/tratamiento farmacológico , Oftalmopatías/etiología , Femenino , Humanos , Inyecciones Intravenosas , Masculino , Persona de Mediana Edad , Enfermedades del Sistema Nervioso/tratamiento farmacológico , Enfermedades del Sistema Nervioso/etiología
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