Clinical and immunological characteristics of opportunistic infections in children with the natural course of HIV infection, taking into account the route of infection

V. Denisenko, E. M. Simovanyan
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Abstract

The purpose of the study is to improve the diagnosis and prognosis of opportunistic infections in children infected with HIV by vertical and parenteral routes, taking into account the dynamics of clinical and immunological parameters.Research methods. Clinical and laboratory examinations were carried out in 192 children infected with HIV by the vertical route (91; group I), parenteral route in infancy (44; group II) and over the age of one year (57; group III).Research results. In group I, a rapid development of immunosuppression was observed: mild immunodeficiency was diagnosed at the age of Me 4 (IQI 2—10) months, advanced immunodeficiency — Me 11 ( IQI 6—24.5) months, severe immunodeficiency — Me 23 ( IQI 11— 56) months. Clinical manifestation of opportunistic infections occurred in the first three years of life with a relatively high content of CD4-lymphocytes. Localized bacterial infections (Me 27,5; IQI 21,9–34,1/100 MYO), candidiasis (Me 14,1; IQI 10,2—18,9 / 100 MYO) and generalized infections (Me 5,2; IQI 2,9—8,5 / 100 MYO) had the highest relative incidence rate. In group II, there was a slower progression of immunosuppression (within one to seven years), the addition of opportunistic infections with a lower content of CD4-lymphocytes, in terms of one to nine years, a high relative incidence of herpes simplex infection (Me 12,9; IQI 7,8—14,9 / 100 MYO), herpes zoster (Me 3; IQI 1,5—5,4 / 100 MYO) and pneumocystosis (Me 3,8; IQI 2,1—6,4 / 100 MYO). In group III, there was a slow progression of immunosuppression (within one to eight years), the development of opportunistic infections with a low content of CD4-lymphocytes, in terms of two to ten years, a rarer manifestation of most diseases.Conclusion. These patterns should be taken into account when planning diagnostic, therapeutic and preventive measures in children with HIV infection, taking into account the path and age at the time of infection.
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机会性感染儿童的临床和免疫学特点与HIV感染的自然过程,同时考虑到感染途径
本研究的目的是在考虑临床和免疫学参数动态的情况下,提高通过垂直和肠外途径感染艾滋病毒的儿童机会性感染的诊断和预后。研究方法。通过垂直路径对192名感染艾滋病毒的儿童进行了临床和实验室检查(91;I组),婴儿期肠外途径(44例;II组)及1岁以上(57岁;第三组).研究结果。在I组中,免疫抑制发展迅速:轻度免疫缺陷在me4 (IQI 2-10)个月时被诊断,重度免疫缺陷- me11 (IQI 6-24.5)个月,重度免疫缺陷- me23 (IQI 11 - 56)个月。机会性感染的临床表现多见于3岁前,cd4 -淋巴细胞含量较高。局部细菌感染(Me 27,5;IQI 21,9 - 34,1/100 MYO),念珠菌病(Me 14,1;IQI 10,2 - 18,9 / 100 MYO)和全身性感染(Me 5,2;IQI 2,9 ~ 8,5 / 100 MYO)的相对发病率最高。在II组中,免疫抑制的进展较慢(1 - 7年),加上cd4淋巴细胞含量较低的机会性感染,在1 - 9年期间,单纯疱疹感染的相对发生率较高(me12,9;IQI 7,8 - 14,9 / 100 MYO),带状疱疹(me3;IQI 1,5 - 5,4 / 100 MYO)和肺囊虫病(Me 3,8;[2][1][6][4]。III组免疫抑制进展缓慢(1 ~ 8年),出现cd4 -淋巴细胞含量低的机会性感染(2 ~ 10年),是大多数疾病的罕见表现。在规划感染艾滋病毒儿童的诊断、治疗和预防措施时,应考虑到这些模式,同时考虑到感染途径和感染时的年龄。
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