Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Analysis of treatment for HIV-infected patients considering CD4 T cell count in STI

Authors
Park, Ki YeonChung, Han ByulChung, Chung Choo
Issue Date
Oct-2006
Publisher
IEEE
Keywords
CD4 T cell count; CTLp; LTNP; STI
Citation
2006 SICE-ICASE International Joint Conference, pp.5247 - 5252
Indexed
SCOPUS
Journal Title
2006 SICE-ICASE International Joint Conference
Start Page
5247
End Page
5252
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/180875
DOI
10.1109/SICE.2006.315831
ISSN
0000-0000
Abstract
Determining drug dosage for STI (Structured Treatment Interruption) according to the clinically healthy CD4 T cell count has recently been proposed due to its simple scheduling and effectiveness. In this paper, we investigated its effectiveness and validity from a mathematical biological point of view and analyzed the human immune system based on a mathematical model of a HIV-infected patient. Compared to the previous STI methods, we found that STI determined by the healthy CD4 T cell count not only reduces the entire treatment period but also the total drug dose administered. We also observed that this type of STI has a continued increase of the CTLp count, which is a vital force to the human self immune system. Therefore, the CTLp count continuously increases and approaches the value of the equilibrium point even after the treatment is terminated so that LTNP is induced. We also found that the base line of CD4 T cells selected to ensure the continued increase of the CTLp count will reduce the risk of opportunistic infection.
Files in This Item
Go to Link
Appears in
Collections
서울 공과대학 > 서울 전기공학전공 > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Chung, Chung Choo photo

Chung, Chung Choo
COLLEGE OF ENGINEERING (MAJOR IN ELECTRICAL ENGINEERING)
Read more

Altmetrics

Total Views & Downloads

BROWSE