AdDRESSing T-cell responses to antituberculous drugs

نویسندگان

  • R. Pavlos
  • A. Redwood
  • E. Phillips
چکیده

In this issue of the BJD, Ye et al.1 present data on T-cell-specific responses in patients with antituberculosis drug (ATD)-induced maculopapular exanthema (MPE) and drug reaction with eosinophilia and systemic symptoms (DRESS). Understanding these responses helps further our knowledge of the immunopathogenesis of antituberculous hypersensitivity, and ideally it would be translated into diagnostic tests that improve ATD drug safety and guide therapy. Isoniazid, rifampicin, pyrazinamide and ethambutol are the first-line therapy used in the first 2 months to treat tuberculosis (TB) and multiple medications make the identification of culprit drugs difficult in the clear diagnosis of adverse drug reactions (ADRs). This uncertainty has detrimental effects, including interruption of treatment for prolonged periods, systemic corticosteroid use and alternative treatment with less effective regimens.2 To confirm the diagnosis of suspected immunologically-mediated ADRs associated with ATD therapy, a combination of skin tests (prick and intradermal dilutional testing) and patch testing is most often employed in the clinic. However, the specificity and sensitivity of patch testing is dependent on both the host and the offending drug and few validation studies exist. In the cases presented by Ye et al.1 patch testing is shown to be of little utility in DRESS and is unsuitable for cases of MPE; however, the oral provocation test and lymphocyte transformation test show a stronger correlation and support multiple drug reactivity.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

In Vivo and In Vitro Effects of Antituberculosis Treatment on Mycobacterial Interferon-γ T Cell Response

BACKGROUND In recent years, the impact of antituberculous treatment on interferon (IFN)-gamma response to Mycobacterium tuberculosis antigens has been widely investigated, but the results have been controversial. The objective of the present study was: i) to evaluate longitudinal changes of IFN-gamma response to M. tuberculosis-specific antigens in TB patients during antituberculous treatment b...

متن کامل

Synergistic effect of \'Y-interferon and chemotherapeutic drugs on KE-37

Therapeutic use of biological response modulators in combination with chemotherapeutic drugs may propose a more efficient way for cancer therapy with fewer side effects. However, the related mechanism has not been well understood. Γ-interferon is a modulator of biological responses that inhibits the growth of malignant cells and mediates their differentiation. In this investigation, T cell lymp...

متن کامل

O-31: Mifepristone Acts as Progesterone Antagonistof Non-Genomic Responses but InhibitsPhytohemagglutinin Induced Proliferationin Human T Cells

Background: Progesterone is an endogenous immunomodulator that suppresses T cell activation during pregnancy. The stimulation of membrane progesterone receptors (mPRs) would seem to be the cause of rapid non-genomic responses in human peripheral T cells, such as an elevation of intracellular calcium ([Ca2+] i) and decreased intracellular pH (pHi). Mifepristoneimmune cells compared with progeste...

متن کامل

Interferon-γ release assay in HIV-infected patients with active tuberculosis: impact of antituberculous drugs on host immune response.

The objective of the study was to: 1) investigate the performance of QuantiFERON-TB Gold In-Tube (QFT-GIT) in HIV-infected patients with active tuberculosis (TB); 2) evaluate the sequential changes in QFT-GIT assay during the treatment response; 3) investigate the direct in vitro effects of antituberculous drugs on both secretion of IFN-g and apoptosis of T cells. Forty-four HIV-patients with a...

متن کامل

Apoptosis and T cell hyporesponsiveness in pulmonary tuberculosis.

Mycobacterium tuberculosis (MTB)-induced T cell responses are depressed in peripheral blood mononuclear cells of persons with newly diagnosed pulmonary tuberculosis (TB), and levels of interferon (IFN)-gamma remain low even after completion of antituberculous therapy. Loss of MTB-reactive T cells through apoptotic mechanisms could account for this prolonged T cell hyporesponsiveness. T cell apo...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 176  شماره 

صفحات  -

تاریخ انتشار 2017