|No T Cells, No Meds, High VL
Jul 4, 2004
I will try to make this as brief as possible, but I have not seen anybody else whose disease has followed a similar path. I have been positive since at least 1992. My T-Cells have been less than 50 for 8 years. I have never had an undetectable viral load and am resistant to every med out there. I have had kidney failure twice (due to meds). I lost my right eye and sinuses to aspergillus 5 years ago. It was lodged in my sinuses and I was told that I was a dead man (had no T cells at the time of surgery), but they took out the eye and treated my with IV amphotericin for a long time, which somehow I tolerated. I survived and am doing quite well. I have gained back all the weight I lost. I feel strong and have not had another OI since then except that I have CMV retinitis in my left eye which has been controlled first with injections and now it has been totally suppressed by Valcyte for the past 2 years. My current CD4 level is 2, VL is 150000. For AIDS meds, I have been taking 3TC only, since my last kidney failure 2 years ago. I also take Bactrim, Diflucan, Sporanox, Biaxin, Cipro and Valtrx. My Doc says the 3TC will keep my virus weakened, rather than allow the more dangerous wild type to reemerge. My Doc wants me to start on T-20 and Tripranivir. I question whether or not to go back on meds at all, since I do not see my health declining at this moment and I feel that maybe I should wait until I really need these drugs rather than starting them now and possibly using up what could be the only two drugs that I may not be resistant to. My question is two-fold. First, have you heard of any other case like mine and secondly, do you think I should go on these meds now or wait until later? Thanks for all the help you have provided to our community over the years.
| Response from Dr. Holodniy
You are to be commended on your courage. Your case is indeed complicated, but not unheard of. The decision to restart additional meds requires some careful thought. To insure success when using t-20 containing regimens requires that at least one, preferably two additional agents are added that have potent activity. If your resistance profile does not indicate this, or tipranavir is already compromised based on protease mutations or cross-resistance to other PIs, then it may not be worth it and you should wait. My first inclination would be to get you on something to get your CD4 count up a bit more, so you are not at such a great risk for further OIs. However, I would not want to sacrafice a new agent like t-20 unless I could maximize the potency of the new regimen.
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