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DOI 10.1007/s00467-017-3796-z

Медицинская библиотека · Pediatric nephrology (Berlin, Germany) · 2017

FOXP3+ T cells are present in kidney biopsy samples in children with tubulointerstitial nephritis and uveitis syndrome.

Rytkönen Sari H, Kulmala Petri, Autio-Harmainen Helena, Arikoski Pekka, Endén Kira, Kataja Janne, Karttunen Tuomo, Nuutinen Matti, Jahnukainen Timo

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Tubulointerstitial nephritis (TIN) is an inflammatory disease of unknown pathogenesis. To evaluate a possible role of regulatory T cells (Tregs) in the pathophysiology of TIN with (TINU) and without uveitis, we investigated the presence and quantity of FOXP3+ T regulatory lymphocytes in diagnostic kidney biopsies from pediatric patients.

METHODS

A total of 33 patients (14 TIN and 19 TINU) were enrolled. The quantity of CD4+, FOXP3+ and double-positive T cells in formalin-fixed kidney biopsies was determined using double label immunohistochemistry with anti-human CD4 and FOXP3 antibodies.

RESULTS

FOXP3 staining was successful in all 33 patients. In patients with chronic uveitis, the density of FOXP3+ cells was significantly lower (p = 0.046) than in TIN patients without uveitis or with uveitis lasting <3 months. CD4+ staining was successful in 23 patients. The density of all lymphocytes (CD4+, CD4+FOXP3+ and FOXP3+ cells) was significantly lower (p = 0.023) in patients with chronic uveitis than in other patients.

CONCLUSIONS

FOXP3+ T cells are present in kidney biopsy samples from TIN and TINU patients. In patients with chronic uveitis, the density of FOXP3+ T cells is significantly lower than in other patients, suggesting a different pathomechanism for these clinical conditions.

Для цитирования: Rytkönen Sari H, Kulmala Petri, Autio-Harmainen Helena, Arikoski Pekka, Endén Kira, Kataja Janne, Karttunen Tuomo, Nuutinen Matti, Jahnukainen Timo. FOXP3+ T cells are present in kidney biopsy samples in children with tubulointerstitial nephritis and uveitis syndrome.. Pediatric nephrology (Berlin, Germany). 2017. DOI: 10.1007/s00467-017-3796-z.

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