Low serum immunoglobulin G2 levels in infancy can be transient

被引:6
作者
Atkinson, Adelle R.
Roifman, Chaim M.
机构
[1] Hosp Sick Children, Infect Immun Injury & Repair Program, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Hosp Sick Children, Jeffrey Modell Res Lab Diag Primary Immunodeficie, Canadian Ctr Primary Immunodeficiency,Div Immunol, Toronto, ON M5G 1X8, Canada
关键词
primary immunodeficiency; immunoglobulin IgG subclasses; childhood; infections;
D O I
10.1542/peds.2006-3613
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVE. The immunoglobulin G(2) subclasses contain predominantly antipolysaccharide antibodies. It was therefore believed intuitively that low immunoglobulin G2 levels could predispose individuals to infections with encapsulated bacteria. Although many reports initially supported this notion, more recent studies challenged it. Regardless of the biological significance, the natural history of low immunoglobulin G2 levels has not been carefully studied. METHODS. We studied the outcome of low serum immunoglobulin G2 subclass levels in children. Thirteen patients who were referred because of recurrent infections were found to have low immunoglobulin G2 levels. Laboratory evaluation at presentation and follow-up visits included total serum immunoglobulins, immunoglobulin subclasses, and specific antibodies to protein antigens and to pneumococcal vaccine. RESULTS. Low immunoglobulin G2 levels resolved completely within 0.6 years to 6 years ( median: 1.5 years) in all patients. All 13 patients responded adequately to vaccination with protein antigens such as tetanus toxoid and polio as well as to immunization with pneumococcal vaccine. Four of 13 patients had a previous history of transient hypogammaglobulinemia, raising the possibility that the other cases may simply represent the tail end of this condition. CONCLUSION. We have demonstrated that low immunoglobulin G2 detected in early infancy and childhood is likely to resolve completely within several months and up to 6 years from the time of presentation.
引用
收藏
页码:E543 / E547
页数:5
相关论文
共 28 条
  • [11] INSEL RA, 1988, MONOGR ALLERGY, V23, P128
  • [12] LEFRANC MP, 1991, IMMUNODEFIC REV, V2, P256
  • [13] MANCINI G, 1964, 9 C PROT BIOL FLUIDS, P370
  • [14] PRESENCE AND ORIGIN OF HUMAN IGG SUBCLASS PROTEINS IN NEWBORNS
    MELLBYE, OJ
    NATVIG, JB
    [J]. VOX SANGUINIS, 1973, 24 (03) : 206 - 215
  • [15] METABOLIC PROPERTIES OF IGG SUBCLASSES IN MAN
    MORELL, A
    TERRY, WD
    WALDMANN, TA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1970, 49 (04) : 673 - &
  • [16] IGG SUBCLASSES - DEVELOPMENT OF SERUM CONCENTRATIONS IN NORMAL INFANTS AND CHILDREN
    MORELL, A
    SKVARIL, F
    HITZIG, WH
    BARANDUN, S
    [J]. JOURNAL OF PEDIATRICS, 1972, 80 (06) : 960 - +
  • [17] NAHM MH, 1986, J IMMUNOL, V137, P3484
  • [18] Natvig J B, 1973, Adv Immunol, V16, P1, DOI 10.1016/S0065-2776(08)60295-3
  • [19] IGG SUBCLASSES IN SELECTIVE IGA DEFICIENCY - IMPORTANCE OF IGG2-IGA DEFICIENCY
    OXELIUS, VA
    LAURELL, AB
    LINDQUIST, B
    GOLEBIOWSKA, H
    AXELSSON, U
    BJORKANDER, J
    HANSON, LA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (24) : 1476 - 1477
  • [20] OXELIUS VA, 1974, CLIN EXP IMMUNOL, V17, P19