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final program.qxd - Parallels Plesk Panel

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PP 3.27<br />

HIV-positive cases as part of viral complications after renal allotransplantation<br />

KT Metodiev¹, PG Lazarova², VI Driyanskaya³<br />

1<br />

Dept.Immunology, Medical University, Varna-Bulgaria; 2 Clin.laboratory, District hospital<br />

"St.Anna", Varna-Bulgaria; 3-Lab.immunology, Inst.Urology&Nephrology, Kiev-Ukraine<br />

Background<br />

It is well-known that recipients of renal allografts suffer from two major complications after<br />

transplantation: rejection crisis and infections. The rejection process is a well-expressed<br />

immune conflict. The infectious processes have various etiology but most often are the<br />

viral ones, followed by bacterial and fungial.<br />

Objectives<br />

It is very essential that a proper, rapid and precise diagnosis, as well as a realistic<br />

prediction of the two postoperative complications, must be performed because they<br />

require rather different therapeutical behaviour.<br />

Materials and methods<br />

The authors of the present study examine dynamically 128 recipients of renal allografts<br />

(before and after transplantation, twice weekly during the first month postoperatively, twice<br />

monthly for the period of the first year) by using both, the immunologic monitoring (IM) and<br />

virologic methods (VM), trying to analyse the possibilities for diagnosis and prognosis of<br />

rejection and infections, also to investigate the etiology of viral processes. The IM includes<br />

basic immune tests for cellular, humoral, specific and nonspecific immunity, type of<br />

immunoreactivity and current immunomodulation, whereas the VM are directed to<br />

antibody and antigen identifiction, also HIV-serologically positive recipients and<br />

HIV-virocarriers (patients on haemodialysis before renal allotransplantation and patients<br />

after operation) by using ELISA.<br />

Results and conclusions<br />

Based on the results the authors suggest that the applied model of IM allow statistically<br />

reliable exact differentiation and prediction (!) of both complications (rejection and<br />

infections). As for the viral infections (altogether 58 for the whole group of 128 recipients),<br />

the following etiology is registered: hepatitis (21 cases or 36.2%), CMV (11 or 18.9%),<br />

Influenza (9 or 15.5%), Adenoviral (4 or 6.9%), ECHO (2 or 3.45%), HIV-serologically<br />

positive cases (3 or 5.2%), from them HIV-virocarriers (2 or 3.45), mixed viral infections<br />

(6 or 10.4%). The immunoreactivity type of the recipients shows that the lower the<br />

immune status is, the oftener are the infections, especially those with viral origin.<br />

Expressed immunodeficiency is registered in 7 cases (CMV-2, Influenza-1, mixed viral<br />

infection-1 and HIV-3). Detailed analysis of the therapy (antiinfective and<br />

immunosuppressive) for both posttransplantation complications is proposed. The model of<br />

IM allows a very reliable analysis and prediction of the immune conflict or infections in the<br />

postoperative periods, thus giving a precise idea for the exact therapy of allograft patients.<br />

“ Focusing FIRST on PEOPLE “ 168 w w w . i s h e i d . c o m

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