Long-Acting HIV Fusion Inhibitor Albuvirtide is A Safe And Effective Treatment in HIV Patients with Severe Liver Impairment, HBV Co-Infection and High HIV RNA Copies

2021 ◽  
Vol 8 (1) ◽  
pp. 1-9
Author(s):  
Feilong Xu
Author(s):  
Giuseppe Castaldo ◽  
Emilia Rippa ◽  
Donatello Salvatore ◽  
Raffaella Sibillo ◽  
Valeria Raia ◽  
...  

2014 ◽  
Vol 17 ◽  
pp. 19718
Author(s):  
Chiara Dentone ◽  
Daniela Fenoglio ◽  
Alessio Signori ◽  
Giovanni Cenderello ◽  
Alessia Parodi ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-5 ◽  
Author(s):  
Shahla Bari ◽  
Jameel Muzaffar ◽  
Austin Chan ◽  
Sanjay R. Jain ◽  
Ahmad M. Haider ◽  
...  

Due to HAART and consequent decline in mortality from infectious complications, HIV patients have an increasing burden of non-AIDS defining cancers. Data on their safety and efficacy is unknown as these patients were excluded from clinical trials due to concern of unforeseen side effects. Objectives. The main objective of our study was to evaluate the efficacy and safety profile of PD-1 and PD-L1 inhibitors in HIV patients being treated for advanced cancers and to assess the impact of these drugs on HIV status of the patients specifically CD4 count and HIV viral load. Materials and Methods. This was a retrospective analysis of data of 17 patients HIV treated with one of the PD-1/PD-L1 inhibitors (Nivolumab, Pembrolizumab, Atezolizumab, Durvalumab, or Avelumab) for advanced cancer. Results. 10 out of 17 patients responded to therapy. 7 patients, all of whom had shown response to therapy, were alive and 4 were still on checkpoint inhibitor. 10 patients including all 7 nonresponders had died. Responders had minimum of 15 weeks of response while one had ongoing continued response at 34 weeks. Side effects were seen in 7 patients and only one patient needed cessation of therapy. CD4 counts were stable on treatment while HIV RNA remained undetectable. Conclusion. PD-1 and PD-L1 inhibitors appear to have comparable efficacy and tolerable side effect profile and have no effect on HIV markers when used in HIV patients with advanced cancers.


PLoS ONE ◽  
2019 ◽  
Vol 14 (10) ◽  
pp. e0224510
Author(s):  
Gloria Samperiz ◽  
Francisco Fanjul ◽  
Jose Luis Valera ◽  
Meritxell Lopez ◽  
Ángel Rios ◽  
...  

2018 ◽  
Vol 209 (6) ◽  
pp. 279-280
Author(s):  
Venessa Pattullo ◽  
Gavin G Pattullo ◽  
Simone I Strasser

Viruses ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 811 ◽  
Author(s):  
Chen Wang ◽  
Shuihong Cheng ◽  
Yuanyuan Zhang ◽  
Yibo Ding ◽  
Huihui Chong ◽  
...  

The clinical application of HIV fusion inhibitor, enfuvirtide (T20), was limited mainly because of its short half-life. Here we designed and synthesized two PEGylated C34 peptides, PEG2kC34 and PEG5kC34, with the PEG chain length of 2 and 5 kDa, respectively, and evaluated their anti-HIV-1 activity and mechanisms of action. We found that these two PEGylated peptides could bind to the HIV-1 peptide N36 to form high affinity complexes with high α-helicity. The peptides PEG2kC34 and PEG5kC34 effectively inhibited HIV-1 Env-mediated cell–cell fusion with an effective concentration for 50% inhibition (EC50) of about 36 nM. They also inhibited infection of the laboratory-adapted HIV-1 strain NL4-3 with EC50 of about 4–5 nM, and against 47 HIV-1 clinical isolates circulating in China with mean EC50 of PEG2kC34 and PEG5kC34 of about 26 nM and 32 nM, respectively. The plasma half-life (t1/2) of PEG2kC34 and PEG5kC34 was 2.6 h and 5.1 h, respectively, and the t1/2 of PEGylated C34 was about 2.4-fold and 4.6-fold longer than C34 (~1.1 h), respectively. These findings suggest that PEGylated C34 with broad-spectrum anti-HIV-1 activity and prolonged half-life can be further developed as a peptide fusion inhibitor-based long-acting anti-HIV drug for clinical use to treat HIV-infected patients who have failed to respond to current anti-retrovirus drugs.


2006 ◽  
Vol 26 (10) ◽  
pp. 1225-1233 ◽  
Author(s):  
Aezam Katoonizadeh ◽  
Frederik Nevens ◽  
Chris Verslype ◽  
Jacques Pirenne ◽  
Tania Roskams

1987 ◽  
Vol 96 (6) ◽  
pp. 554-558 ◽  
Author(s):  
Charles I. Woods ◽  
Duncan S. Postma ◽  
Jiri Prazma ◽  
James Sidman

Several studies recommend the use of steroids and racemic epinephrine for treatment of postintubation croup. Few controlled clinical or laboratory studies, however, support their effectiveness, and many questions remain about their use. The present study was undertaken to develop a reproducible animal model for postintubation croup and to perform initial controlled studies of the effects of dexamethasone (4 mg/kg) and the long-acting vasoconstrictor oxymetazoline (0.01 solution). An animal model for intubation trauma was developed with ten 10-week-old ferrets. Two models were created to reflect the spectrum of trauma—from simple mucosal contusion to mucosal ulceration. The first was to surgically strip mucosa in a circumferential manner at the level of the cricoid ring; the second was intubation trauma to the glottic and subglottic regions by use of a circular brush. Neither dexamethasone nor oxymetazoline had any statistically significant effect on subglottic edema in the mucosal stripping model. In the brush intubation model, oxymetazoline decreased subglottic edema at 2, 4, and 8 hours ( P < 0.05), while dexamethasone and combination therapy decreased edema at 2,4, 8, and 24 hours ( P < 0.05). At 24 hours, combination therapy was demonstrated to be the most effective in reducing subglottic edema. Oxymetazoline was as effective as dexamethasone and combination therapy at 2, 4, and 8 hours ( P < 0.05). In this preliminary study, we have established the potential usefulness of the brush intubation model for the study of this disorder. This model was shown to have a reproducible and reversible lesion. The mucosal stripping model was not shown to have reversible lesion and—while further study needs to be performed—may only be useful as a model for very severe cases of this disorder. These initial studies also demonstrated high-dose dexamethasone and oxymetazoline to be effective in treatment of subglottic edema secondary to mucosal trauma. They also indicate that combination therapy is a more effective treatment than either agent alone.


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