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1.
Mediators Inflamm ; 2020: 1747894, 2020.
Article in English | MEDLINE | ID: mdl-33132753

ABSTRACT

Recent evidence suggests that abnormalities involving CD4+T lymphocytes are associated with the pathophysiology of osteonecrosis (ON); however, few studies have addressed the CD4+T cells in ON related to sickle cell disease (SCD/ON). In addition, T cells producing multiple cytokines simultaneously are often present in the inflammatory milieu and may be implicated in the immune response observed in SCD/ON. In the present study, we aimed to characterize the functional status of CD4+T cells in SCD by simultaneously determining the frequency of IFN-γ +, IL-4+, and IL-17+ CD4+T in cell cultures under exogenous stimuli. Peripheral blood mononuclear cells (PB-MNCs) from 9 steady-state SCD patients, 15 SCD/ON patients, and 19 healthy controls had functional status of CD4+T cells analyzed. Bone marrow mononuclear cells (BM-MNCs) from 24 SCD/ON patients (SCD BM) and 18 patients with ON not related to SCD (non-SCD BM) were also analyzed. We found that PB-MNC of SCD patients with or without ON presented significantly reduced TCD4+, TCD8+, and TCD4+ naïve cell frequencies and increased frequency of circulating CD4+T cells able to simultaneously produce IFN-γ +/IL4+ and IL-17+/IL4+ compared to healthy controls. Conversely, the polyclonal stimulation of BM-MNC induced an increased frequency of CD4+IFN-γ + and CD4+IL-17+ in SCD BM compared to non-SCD BM. The increased proportion of CD4+ T cells able to produce a broad spectrum of proinflammatory cytokines after a strong stimulus indicates that the immune system in SCD/ON patients presents an expressive pool of partially differentiated cells ready to take on effector function. It is possible that this increased subpopulation may extend to inflammatory sites of target organs and may contribute to the maintenance of inflammation and the pathophysiology of osteonecrosis in sickle cell disease.


Subject(s)
Anemia, Sickle Cell/immunology , Anemia, Sickle Cell/metabolism , CD4-Positive T-Lymphocytes/metabolism , Osteonecrosis/immunology , Osteonecrosis/metabolism , Adolescent , Adult , Female , Hematopoietic Stem Cells/metabolism , Hemoglobins/metabolism , Humans , Immunophenotyping , Interferon-gamma/metabolism , Interleukin-17/metabolism , Interleukin-4/metabolism , Male , Middle Aged , Young Adult
2.
J. bras. patol. med. lab ; 42(6): 437-440, dez. 2006. ilus
Article in Portuguese | LILACS | ID: lil-446498

ABSTRACT

A ocronose, manifestação clínica da alcaptonúria nos tecidos conectivos, geralmente leva a uma degeneração discal grave, com quadro radiológico exuberante e pouca sintomatologia, sendo o tratamento cirúrgico raramente necessário. Este trabalho relata o caso de um paciente com ocronose que desenvolveu uma radiculopatia em L5, à esquerda, secundária a hérnia discal paramediana esquerda, entre L4 e L5, que não melhorou com o tratamento fisioterápico efetuado durante quatro meses. Optou-se por tratamento cirúrgico com discectomia isolada, e o resultado foi o desaparecimento dos sintomas da radiculopatia em L5, sem recidiva nos 26 meses subsequentes de acompanhamento.


Ochronosis, alkaptonuric clinical presentation in connective tissues, often runs with severe disc degeneration. In these patients, symptoms and clinical signs of disc degeneration usually are not as prominent as might be expected from the extent of disease observed on X-ray, and discectomy is rarely needed. We report a case of disc herniation in an ochronotic patient with left L5 radiculopathy, with symptoms and clinical signs not responsive to 4-month physical therapy. Discectomy was performed, with sustained good results after a 26-month follow-up.


Subject(s)
Humans , Male , Adult , Alkaptonuria/surgery , Alkaptonuria/pathology , Intervertebral Disc Displacement/surgery , Ochronosis/surgery , Ochronosis/pathology , Lumbar Vertebrae/pathology , Radiculopathy/pathology
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