Patency of Litomosoides sigmodontis infection depends on T oll‐like receptor 4 whereas T oll‐like receptor 2 signalling influences filarial‐specific CD 4 + T‐cell responses
BALB /c mice develop a patent state [release of microfilariae (Mf), the transmission life‐stage, into the periphery] when exposed to the rodent filariae Litomosoides sigmodontis . Interestingly, only a portion of the infected mice become patent, which reflects the situation in human individuals infe...
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Veröffentlicht in: | Immunology 2016-04, Vol.147 (4), p.429-442 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | BALB
/c mice develop a patent state [release of microfilariae (Mf), the transmission life‐stage, into the periphery] when exposed to the rodent filariae
Litomosoides sigmodontis
. Interestingly, only a portion of the infected mice become patent, which reflects the situation in human individuals infected with
Wuchereria bancrofti
. Since those individuals had differing filarial‐specific profiles, this study compared differences in immune responses between Mf
+
and Mf
–
infected
BALB
/c mice. We demonstrate that cultures of total spleen or mediastinal lymph node cells from Mf
+
mice produce significantly more interleukin‐5 (
IL
‐5) to filarial antigens but equal levels of
IL
‐10 when compared with Mf
–
mice. However, isolated
CD
4
+
T cells from Mf
+
mice produced significantly higher amounts of all measured cytokines, including
IL
‐10, when compared with
CD
4
+
T‐cell responses from Mf
–
mice. Since adaptive immune responses are influenced by triggering the innate immune system we further studied the immune profiles and parasitology in infected Toll‐like receptor‐2‐deficient (
TLR
2
−/−
) and
TLR
4
−/−
BALB
/c mice. Ninety‐three per cent of
L. sigmodontis
‐exposed
TLR
4
−/−
BALB
/c mice became patent (Mf
+
) although worm numbers remained comparable to those in Mf
+
wild‐type controls. Lack of
TLR
2 had no influence on patency outcome or worm burden but infected Mf
+
mice had significantly lower numbers of Foxp3
+
regulatory T cells and dampened peripheral immune responses. Interestingly,
in vitro
culturing of
CD
4
+
T cells from infected wild‐type mice with granulocyte–macrophage colony‐stimulating factor‐derived
TLR
2
−/−
dendritic cells resulted in an overall diminished cytokine profile to filarial antigens. Hence, triggering
TLR
4 or
TLR
2 during chronic filarial infection has a significant impact on patency and efficient
CD
4
+
T‐cell responses, respectively. |
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ISSN: | 0019-2805 1365-2567 |
DOI: | 10.1111/imm.12573 |