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婴儿暂时性低丙种球蛋白血症患者缺乏特异性病毒抗体。

Absent specific viral antibodies in patients with transient hypogammaglobulinemia of infancy.

作者信息

Cano F, Mayo D R, Ballow M

机构信息

University of Connecticut Health Center, Department of Pediatrics, Farmington.

出版信息

J Allergy Clin Immunol. 1990 Feb;85(2):510-3. doi: 10.1016/0091-6749(90)90163-x.

Abstract

Of 247 patients referred to the Pediatric Immunology Clinic, University of Connecticut Health Center, Farmington, Conn., for recurrent infections, 13 patients were found to have an abnormal delay in the onset of IgG synthesis and prolongation of the physiologic hypogammaglobulinemia of infancy. At first observation, their mean age was 10.6 months. All patients had abnormally low serum IgG levels (less than or equal to 2 SD for their age). The mean serum IgG level for our patient population was 270 +/- 81 mg/dl; the mean serum IgG level of the control group was 749 +/- 440 mg/dl. Clinically, these patients were first observed with recurrent otitis media, respiratory infections, bronchitis and/or asthma, and formula intolerance. Despite recurrent respiratory tract infections, specific antibodies to the respiratory viruses were absent in nine of 11 patients tested who were observed before 17 months of age. On follow-up, two of the 13 patients never developed specific antibodies to viral agents, although their serum IgG levels normalized; one patient became serology positive at the same time that the serum IgG normalized. In two patients, the serum IgG levels returned to within the normal range for age before the appearance of specific viral antibodies. In eight patients, the appearance of specific viral antibodies was detected before the serum IgG levels returned to normal. Five of these eight patients were treated for short periods (9 months) with replacement immune serum globulin (intramuscular) therapy and did clinically well. These observations suggest that replacement immune serum globulin for short periods of time does not appear to suppress the production of specific, naturally occurring antibodies and the resolution of the hypogammaglobulinemia.

摘要

在转诊至康涅狄格大学健康中心法明顿分校儿科免疫诊所的247例因反复感染前来就诊的患者中,发现13例患者存在IgG合成起始异常延迟以及婴儿生理性低丙种球蛋白血症期延长的情况。初次观察时,他们的平均年龄为10.6个月。所有患者的血清IgG水平均异常低下(低于或等于其年龄对应的2个标准差)。我们患者群体的平均血清IgG水平为270±81mg/dl;对照组的平均血清IgG水平为749±440mg/dl。临床上,这些患者最初表现为反复中耳炎、呼吸道感染、支气管炎和/或哮喘,以及对配方奶不耐受。尽管有反复的呼吸道感染,但在17个月前接受观察的11例接受检测的患者中,有9例缺乏针对呼吸道病毒的特异性抗体。随访发现,13例患者中有2例尽管血清IgG水平恢复正常,但从未产生针对病毒制剂的特异性抗体;1例患者在血清IgG恢复正常的同时血清学转为阳性。在2例患者中,血清IgG水平在特异性病毒抗体出现之前就已恢复到年龄正常范围内。在8例患者中,在血清IgG水平恢复正常之前就检测到了特异性病毒抗体。这8例患者中有5例接受了短期(9个月)的替代免疫血清球蛋白(肌肉注射)治疗,临床效果良好。这些观察结果表明,短期使用替代免疫血清球蛋白似乎不会抑制特异性天然抗体的产生以及低丙种球蛋白血症的缓解。

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