Lymphocyte homing to bronchus-associated lymphoid tissue (BALT) is mediated by L-selectin/PNAd, α4β1 integrin/VCAM-1, and LFA-1 adhesion pathways

被引:133
作者
Xu, BH
Wagner, N
Pham, LN
Magno, V
Shan, ZY
Butcher, EC [1 ]
Michie, SA
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[2] Palo Alto Hlth Care Syst, Dept Vet Affairs, Pathol & Lab Med Serv, Palo Alto, CA 94304 USA
[3] Kagoshima Univ, Fac Med, Dept Environm Med, Kagoshima 8908520, Japan
[4] City Hosp Dortmund, Dept Pediat, D-44137 Dortmund, Germany
关键词
lung; bronchi; cell adhesion molecules; endothelium; CD106;
D O I
10.1084/jem.20010685
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bronchus-associated lymphoid tissue (BALT) participates in airway immune responses. However, little is known about the lymphocyte-endothelial adhesion cascades that recruit lymphocytes from blood into BALT. We show that high endothelial venules (HEVs) in BALT express substantial levels of VCAM-1, in marked contrast to HEVs in other secondary lymphoid tissues. BALT HEVs also express the L-selectin ligand PNAd. Anti-L-selectin, anti-PNAd, and anti-LFA-1 mAbs almost completely block the homing of B and T lymphocytes into BALT, whereas anti-alpha(4), integrin and anti-VCAM-1 mobs inhibit homing by nearly 40%. alpha(4)beta(7) integrin and MAdCAM-1 are not involved. Importantly, we found that mAbs against alpha(4) integrin and VCAM-1 significantly block the migration of total T cells (80% memory phenotype) but not naive T and B cells to BALT. These results suggest that an adhesion cascade, which includes L-selectin/PNAd, alpha(4)beta(1) integrin/VCAM-1, and LFA-1, targets specific lymphocyte subsets to BALT. This high level of involvement of alpha(4)beta(1) integrin/VCAM-1 is unique among secondary lymphoid tissues, and may help unify lymphocyte migration pathways and immune responses in BALT and other bronchopulmonary tissues.
引用
收藏
页码:1255 / 1267
页数:13
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