Predictive value of CD19 measurements for bacterial infections in children infected with human immunodeficiency virus

被引:4
作者
Betensky, RA
Calvelli, T
Pahwa, S
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[2] Albert Einstein Coll Med, Bronx, NY 10467 USA
[3] NYU, N Shore Hosp, Sch Med, Manhasset, NY 11030 USA
关键词
D O I
10.1128/CDLI.6.2.247-253.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated the predictive value of CD19 cell percentages (CD19%) for times to bacterial infections, using data from six pediatric AIDS Clinical Trials Group protocols and adjusting for other potentially prognostic variables, such as CD4%, CD8%, immunoglobulin (IgA) level, lymphocyte count, prior infections, prior zidovudine treatment, and age. In addition, we explored the combined effects of CD19% and IgG level in predicting time to infection, We found that a low CD19% is associated with a nonsignificant 1.2-fold increase in hazard of bacterial infection (95% confidence interval: 0.97, 1.49), In contrast, a high IgG level is associated with a nonsignificant 0.87-fold decrease in hazard of infection (95% confidence interval: 0.68, 1.12), CD4% was more prognostic of time to bacterial infection than CD19% or IgG level, Low CD19% and high IgG levels together lead to a significant (P < 0.01) 0.50-fold decrease in hazard (95% confidence interval: 0.35, 0.73) relative to low CD19% and low IgG levels. Similarly, in a model involving assay result changes (from baseline to 6 months) as well as baseline values, the effect of CD19% by itself is reversed from its effect in conjunction with IgG, In this model, CD19% that are increasing and high are associated with decreases in hazard of infection (P < 0.01), while increasing CD19% and increasing IgG levels are associated with significant (at the P = 0.01 level) fourfold increases in hazard of infection relative to stable CD19% and decreasing, stable, or increasing IgG levels. Our data suggest that CD19%, in conjunction with IgG level, provides a useful prognostic tool for bacterial infections. It is highly likely that T-helper function impacts on B-cell function; thus, inclusion of CD4% in such analyses may greatly enhance the assessment of risk for bacterial infection.
引用
收藏
页码:247 / 253
页数:7
相关论文
共 14 条
[1]   SPONTANEOUS INVITRO PRODUCTION OF VIRUS-SPECIFIC ANTIBODY BY LYMPHOCYTES FROM HIV-INFECTED SUBJECTS [J].
AMADORI, A ;
DEROSSI, A ;
FAULKNERVALLE, GP ;
CHIECOBIANCHI, L .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1988, 46 (03) :342-351
[2]  
[Anonymous], 1994, Modeling Survival Data in Medical Research
[3]   IMMUNOGLOBULIN-V(H)3 GENE-PRODUCTS - NATURAL LIGANDS FOR HIV GP120 [J].
BERBERIAN, L ;
GOODGLICK, L ;
KIPPS, TJ ;
BRAUN, J .
SCIENCE, 1993, 261 (5128) :1588-1591
[4]   DEFECTIVE HUMORAL IMMUNITY IN PEDIATRIC ACQUIRED IMMUNE-DEFICIENCY SYNDROME [J].
BERNSTEIN, LJ ;
OCHS, HD ;
WEDGWOOD, RJ ;
RUBINSTEIN, A .
JOURNAL OF PEDIATRICS, 1985, 107 (03) :352-357
[5]   Differential regulation of the antibody responses to Gag and Env proteins of human immunodeficiency virus type 1 [J].
Binley, JM ;
Klasse, PJ ;
Cao, YZ ;
Jones, I ;
Markowitz, M ;
Ho, DD ;
Moore, JP .
JOURNAL OF VIROLOGY, 1997, 71 (04) :2799-2809
[6]  
COX DR, 1972, J R STAT SOC B, V34, P187
[7]   INTRAVENOUS IMMUNE GLOBULIN FOR THE PREVENTION OF BACTERIAL-INFECTIONS IN CHILDREN WITH SYMPTOMATIC HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION [J].
MOFENSON, LM .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (02) :73-80
[9]  
PAHWA S, 1990, CRIT CARE MED, V18, P138
[10]   ONTOGENY OF ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) ANTIBODY-PRODUCTION IN HIV-1-INFECTED INFANTS [J].
POLLACK, H ;
ZHAN, MX ;
ILMETMOORE, T ;
AJUANGSIMBIRI, K ;
KRASINSKI, K ;
BORKOWSKY, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (06) :2340-2344