Opsonic requirements for the respiratory burst of neutrophils against Giardia lamblia trophozoites

被引:5
作者
Arbo, A
Pavís-Ruz, N
Santos, JI
机构
[1] Hosp Infantil Mexico Dr Federico Gomez, Dept Infect Dis, Mexico City 06720, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Dept Expt Med, Mexico City 04510, DF, Mexico
关键词
Giardia lamblia; polymorphonuclear neutrophil; respiratory burst; opsonization;
D O I
10.1016/j.arcmed.2005.11.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background. Giardia lamblia is an important cause of parasitic diarrheal disease worldwide. Occasionally, polymorphonuclear neutrophils (PMNs) may participate as effector cells against Giardia lamblia. The present study was performed in order to examine the role of specific antibody and complement components in promoting the respiratory burst (RB) of PMNs against Giardia lamblia. Methods. PMNs from human adult volunteers were incubated with Giardia trophozoites in the presence of non-immune (NS) or hyperimmune (HS) serum (anti-Giardia titer, > 1:1024). Adherence was scored visually on coverslide after staining with Giemsa. The ability of Giardia to trigger the oxidative response of PMNs was measured by the anion superoxide (O-2(-)) production using a cytochrome C reduction method and by the luminol amplified chemiluminescence (CL) assay. Results. Incubation with NS or HS increased Giardia adherence to PMNs from 6.9 +/- 3.2% (basal adherence of Giardia incubated in buffer) to 39 +/- 18.6% (p <0.01) and 76 +/- 19.5% (p <0.001), repectively. In absence of serum, Giardia failed to trigger an oxidative response of PMNs. Opsonization with NS or HS increased the PMN O-2(-) production from 3.9 +/- 0.92 nmol/2.5 x 10(6) PMNs/10 min to 9.04 +/- 1.68 (p <0.05) and 17.9 +/- 1.32 (p <0.001), respectively. A similar enhancement of the CL response was also observed. The inactivation of complement activity by heat as well as the elimination of specific antibodies by absorption produced a significant abrogation of the oxidative response but in the case of HS heat inactivation alone did not abolish the response. Similar findings (variable abrogation of the oxidative PMN response) were observed when PMNs C, were incubated with monoclonal antibodies directed against complement C3, C3b or the low-affinity Fc receptors (CR1, CR3 or FcRlo). Conclusions. These results show that complement components and specific antibodies influence in the Giardia-PMN interaction. Although components of complement can contribute to the RB of PMNs, specific antibodies are critical for an optimal oxidative PMN response. (C) 2006 IMSS. Published by Elsevier Inc.
引用
收藏
页码:465 / 473
页数:9
相关论文
共 48 条
[1]   Giardia intestinalis [J].
Ali, SA ;
Hill, DR .
CURRENT OPINION IN INFECTIOUS DISEASES, 2003, 16 (05) :453-460
[2]  
Arbo A, 1990, Arch Invest Med (Mex), V21 Suppl 1, P57
[3]  
ARBO A, 1989, 4 PAN C INF DIS CAR
[4]   LEUKOKINETIC STUDIES .4. TOTAL BLOOD, CIRCULATING AND MARGINAL GRANULOCYTE POOLS AND GRANULOCYTE TURNOVER RATE IN NORMAL SUBJECTS [J].
ATHENS, JW ;
WINTROBE, MM ;
ASHENBRUCKER, H ;
CARTWRIGHT, GE ;
MAUER, AM ;
HAAB, OP ;
RAAB, SO .
JOURNAL OF CLINICAL INVESTIGATION, 1961, 40 (06) :989-&
[5]   BIOLOGICAL DEFENSE MECHANISMS - PRODUCTION BY LEUKOCYTES OF SUPEROXIDE A POTENTIAL BACTERICIDAL AGENT [J].
BABIOR, BM ;
KIPNES, RS ;
CURNUTTE, JT .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (03) :741-744
[6]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[7]  
BRANDBOR.LL, 1967, GASTROENTEROLOGY, V52, P143
[8]   TUFTSIN DEFICIENCY - NEW SYNDROME WITH DEFECTIVE PHAGOCYTOSIS [J].
CONSTANTOPOULOS, A ;
SMITH, JW ;
NAJJAR, VA .
JOURNAL OF PEDIATRICS, 1972, 80 (04) :564-+
[9]   Availability of complement bound to Staphylococcus aureus to interact with membrane complement receptors influences efficiency of phagocytosis [J].
Cunnion, KM ;
Zhang, HM ;
Frank, MM .
INFECTION AND IMMUNITY, 2003, 71 (02) :656-662
[10]   OPSONIC REQUIREMENTS FOR THE UPTAKE OF CRYPTOCOCCUS-NEOFORMANS BY HUMAN POLYMORPHONUCLEAR LEUKOCYTES AND MONOCYTES [J].
DAVIES, SF ;
CLIFFORD, DP ;
HOIDAL, JR ;
REPINE, JE .
JOURNAL OF INFECTIOUS DISEASES, 1982, 145 (06) :870-874