An enzyme immunoassay to determine the levels of specific antibodies toward bacterial surface antigens in human immunoglobulin preparations and blood serum

被引:23
作者
Lamari, F
Anastassiou, ED
Tsegenidis, T
Dimitracopoulos, G
Karamanos, NK [1 ]
机构
[1] Univ Patras, Dept Chem, Sect Organ Chem Biochem & Nat Prod, GR-26110 Patras, Greece
[2] Univ Patras, Sch Med, Dept Microbiol, GR-26110 Patras, Greece
关键词
bacterial surface antigens; pathogen-specific antibodies; intravenous immunoglobulin; enzyme immunoassay;
D O I
10.1016/S0731-7085(99)00087-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Human polyvalent intravenous immunoglobulin (IVIG) preparations are used as a complementary aid to the proper antimicrobial treatment of severely septic patients in intensive care units (ICUs) and/or as a prophylactic agent to immunocompromized hosts, particularly prone to bacterial infections. There is skepticism about the usefulness of IVIGs since it is not known whether their administration ensures the enhancement of humoral immune responses by providing a sufficient amount of specific antibodies towards the specified bacterial pathogen to be treated. In this report, a simple and reproducible enzyme-linked immunosorbent assay for determining the content of specific antibodies against bacterial surface antigens in commercially available IVIG preparations is described. The method is also easily applied to determine the amount of bacterial antibodies in blood serum. The levels of specific antibodies toward Gram positive and negative pathogenic isolates often encountered in ICUs were estimated in two IVIG (Sandoglobulin(R) and Gamimmune(R)) preparations. Significant differences regarding the content of antibodies to certain clinically bacterial isolates were identified not only between the two IVIG preparations tested, but also among various lots from each IVIG preparation. No significant variation (P less than or equal to 0.001) among the bottles derived from the same lot was determined in both preparations. The variation in the levels of specific antibodies in IVIG preparations may be attributed to differences between the donor pools as well as the manufacturing procedure. Application of the method to patients with primary immune deficiencies showed that infusion of highly reactive IVIG preparations enhanced significantly their humoral response toward various pathogens. The results of this study suggest that the content determination of pathogen-specific antibodies in IVIG preparations before administration may be of great importance for treating bacterial infections. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:913 / 920
页数:8
相关论文
共 18 条
[1]   Opsonic antibodies to the surface M protein of group A streptococci in pooled normal immunoglobulins (IVIG): Potential impact on the clinical efficacy of IVIG therapy for severe invasive group a streptococcal infections [J].
Basma, H ;
Norrby-Teglund, A ;
McGeer, A ;
Low, DE ;
El-Ahmedy, O ;
Dale, JB ;
Schwartz, B ;
Kotb, M .
INFECTION AND IMMUNITY, 1998, 66 (05) :2279-2283
[2]   Antibody-based therapies for emerging infectious diseases [J].
Casadevall, A .
EMERGING INFECTIOUS DISEASES, 1996, 2 (03) :200-208
[3]   Magnitude and prevention of nosocomial infections in the intensive care unit [J].
Fridkin, SK ;
Welbel, SF ;
Weinstein, RA .
INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 1997, 11 (02) :479-+
[4]  
Galama JMD, 1997, J MED VIROL, V53, P273, DOI 10.1002/(SICI)1096-9071(199711)53:3<273::AID-JMV16>3.3.CO
[5]  
2-#
[6]  
HIEMSTRA PS, 1994, J LAB CLIN MED, V123, P241
[7]   The role of intravenous immunoglobulin for the prevention and treatment of neonatal sepsis [J].
Jenson, HB ;
Pollock, BH .
SEMINARS IN PERINATOLOGY, 1998, 22 (01) :50-63
[8]  
Karamanos NK, 1996, INTRAVENOUS IMMUNOGLOBULIN, P345
[9]  
Kemeny DM., 1991, PRACTICAL GUIDE ELIS
[10]   Antibody responses and opsonic activity in sera of preterm neonates with coagulase-negative staphylococcal septicemia and the effect of the administration of fresh frozen plasma [J].
Krediet, TG ;
Beurskens, FJM ;
Van Dijk, H ;
Gerards, LJ ;
Fleer, A .
PEDIATRIC RESEARCH, 1998, 43 (05) :645-651