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Featured researches published by Anis A. Khan.


International Journal of Antimicrobial Agents | 1999

Effect of clarithromycin and azithromycin on production of cytokines by human monocytes

Anis A. Khan; Teri R. Slifer; Fausto G. Araujo; Jack S. Remington

We examined the in vitro effect of clarithromycin and azithromycin on cytokine production by LPS and Pansorbin stimulated human monocytes. At concentrations that are physiologically achievable, both antibiotics affected in vitro production of IL-1alpha, IL-1beta, IL-6, IL-10, GM-CSF and TNF-alpha to varying degrees. Of those individuals in whom a significant increase or decrease in cytokine production was noted, clarithromycin treatment resulted in a significant suppression of production of each cytokine in 71% and a significant increase in 29% of the individuals. Similar results were noted with azithromycin. The results with IL-6 and TNF-alpha in the clarithromycin studies were most striking. A significant decrease was noted in 60% of individuals for IL-6 and 86% for TNF-alpha. For azithromycin, the most interesting results were for IL-1alpha (decrease in 100% of individuals) and for TNF-alpha (decrease in 100% of individuals). These results show that both clarithromycin and azithromycin alter cytokine production in human monocytes and thus possess immunomodulatory activity.


Antimicrobial Agents and Chemotherapy | 2000

Protection against lipopolysaccharide-induced death by fluoroquinolones.

Anis A. Khan; Teri R. Slifer; Fausto G. Araujo; Yasuhiro Suzuki; Jack S. Remington

ABSTRACT Because fluoroquinolones have an immunomodulatory effect on cytokine production by lipopolysaccharide (LPS)-treated human monocytes, we examined the effect of fluoroquinolones on the survival of mice injected with a lethal dose of LPS. Trovafloxacin (100 mg/kg), ciprofloxacin (250 mg/kg), and tosufloxacin (100 mg/kg) protected 75% (P = 0.0001), 25% (P = 0.002), and 50% (P = 0.002), respectively, of mice against death. The fluoroquinolones significantly reduced serum levels of interleukin-6 and tumor necrosis factor alpha in LPS-treated mice. The protective effects of fluoroquinolones in LPS-induced shock in mice may also occur in humans.


Antimicrobial Agents and Chemotherapy | 2001

Activity of Gatifloxacin Alone or in Combination with Pyrimethamine or Gamma Interferon against Toxoplasma gondii

Anis A. Khan; Teri R. Slifer; Fausto G. Araujo; Jack S. Remington

ABSTRACT The activity of gatifloxacin against Toxoplasma gondii, either alone or in combination with pyrimethamine or gamma interferon (IFN-γ), was examined in vitro and in vivo. In vitro, gatifloxacin significantly inhibited intracellular replication of tachyzoites of the RH strain with a 50% inhibitory concentration of 0.21 μg/ml at 48 h after addition of the drug to the cultures. Toxicity for host cells was not observed at this concentration. A synergistic effect (combination indices < 0.5) was demonstrated in vitro following 48 h of treatment with the combination of gatifloxacin and pyrimethamine (1:1 ratio). Doses of gatifloxacin of 100 and 200 mg/kg of body weight/day administered orally to mice for 10 days resulted in significant (P values of 0.056 and <0.0001, respectively) prolongation in time to death following infection with a lethal inoculum of tachyzoites. A dose of 400 mg/kg resulted in 20% survival (P = 0.0001). Mortality was 100% in untreated control mice and in mice treated with 25 or 50 mg/kg/day. Treatment of infected mice with a combination of gatifloxacin at 200 mg/kg/day and pyrimethamine at 12.5 mg/kg/day resulted in 85% survival, whereas 100 and 80% of mice treated with gatifloxacin alone or pyrimethamine alone, respectively, died (P < 0.0001). Moreover, a gatifloxacin dose of 200 mg/kg/day administered orally for 10 days plus 2 μg of recombinant murine IFN-γ/day administered intraperitoneally for 10 days resulted in significant survival compared with IFN-γ alone (P < 0.0001) or gatifloxacin alone (P < 0.007).


The Journal of Infectious Diseases | 2000

Effect of Quinupristin/Dalfopristin on Production of Cytokines by Human Monocytes

Anis A. Khan; Teri R. Slifer; Fausto G. Araujo; Jack S. Remington

The effect of the novel streptogramin antibiotic quinupristin/dalfopristin (synercid) on cytokine production in vitro was examined in monocytes obtained from healthy human volunteers and stimulated with either lipopolysaccharide or heat-killed Staphylococcus aureus (Pansorbin). Synercid at concentrations that are achievable in humans (1, 5, and 10 microgram/mL) significantly suppressed production of interleukin (IL)-1alpha, IL-1beta, IL-6, IL-10, granulocyte-macrophage colony-stimulating factor, and tumor necrosis factor-alpha in a concentration-dependent manner. Thus, synercid possesses significant immunomodulatory activity, in addition to its antimicrobial activity.


Antimicrobial Agents and Chemotherapy | 1998

Effect of Trovafloxacin on Production of Cytokines by Human Monocytes

Anis A. Khan; Teri R. Slifer; Jack S. Remington


Antimicrobial Agents and Chemotherapy | 1996

Trovafloxacin is active against Toxoplasma gondii.

Anis A. Khan; Teri Slifer; Fausto G. Araujo; Jack S. Remington


Antimicrobial Agents and Chemotherapy | 1997

The ketolide antibiotics HMR 3647 and HMR 3004 are active against Toxoplasma gondii in vitro and in murine models of infection.

Fausto G. Araujo; Anis A. Khan; Teri Slifer; Andre Bryskier; Jack S. Remington


Antimicrobial Agents and Chemotherapy | 1996

Rifapentine is active in vitro and in vivo against Toxoplasma gondii.

Fausto G. Araujo; Anis A. Khan; Jack S. Remington


Journal of Antimicrobial Chemotherapy | 1998

Use of ketolides in combination with other drugs to treat experimental toxoplasmosis.

Fausto G. Araujo; Anis A. Khan; A Bryskier; Jack S. Remington


Antimicrobial Agents and Chemotherapy | 1999

Anti-Toxoplasma gondii Activities and Structure-Activity Relationships of Novel Fluoroquinolones Related to Trovafloxacin

Anis A. Khan; Fausto G. Araujo; Katherine E. Brighty; Thomas D. Gootz; Jack S. Remington

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Fausto G. Araujo

Palo Alto Medical Foundation

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Teri R. Slifer

Palo Alto Medical Foundation

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Mohamed Nasr

National Institutes of Health

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