A Randomized, Placebo-controlled, Double-blind Pilot Study of Single-dose Humanized Anti-IL5 Antibody (Reslizumab) for the Reduction of Eosinophilia Following Diethylcarbamazine Treatment of Loa loa Infection

Author:

Legrand Fanny1,Herrick Jesica12,Makiya Michelle1,Ramanathan Roshan13,Thompson Reagan4,Rampertaap Shakuntala5,Stoddard Jennifer5,Ware JeanAnne1,Fay Michael P6,Holland-Thomas Nicole1,Nutman Thomas B1,Klion Amy D1

Affiliation:

1. Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA

2. Division of Infectious Diseases, Immunology and International Medicine, College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA

3. Emergent Biosolutions, Gaithersburg, Maryland, USA

4. University of Virginia Family Medicine, Charlottesville, Virginia, USA

5. Department of Laboratory Medicine, Warren Magnusson Clinical Center, National Institutes of Health, Bethesda, Maryland, USA

6. Division of Clinical Research, Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases, Rockville, Maryland, USA

Abstract

Abstract Background Diethylcarbamazine citrate (DEC) treatment of loiasis is complicated by adverse reactions that are correlated with the number of circulating microfilariae (mf). The cause of these reactions is unknown, but they are accompanied by a dramatic interleukin-5 (IL-5)-dependent increase in eosinophilia and evidence of eosinophil activation. Methods To explore the role of IL-5 driven eosinophilia in post-DEC reactions, 8 adults with confirmed loiasis and <5000 mf/mL blood were enrolled in a randomized, double-blind, placebo-controlled trial of the humanized anti-IL-5 antibody, reslizumab, (1.0 mg/kg IV) administered 3 to 7 days prior to initiation of DEC treatment (9 mg/kg/day for 21 days). The primary endpoint was the reduction in absolute eosinophil count (AEC) during the first week of DEC treatment. Results Baseline characteristics were comparable between the two groups. Single dose reslizumab lowered the AEC by 77% prior to initiation of DEC therapy (vs. 12% in the placebo group, P < .05). More importantly, AEC remained below baseline in the first week of DEC treatment in all subjects who received reslizumab and in none of the placebo subjects. Mf clearance occurred within 2 days of initiation of DEC in all 7 mf-positive subjects. Mild to moderate adverse events were seen in all 8 subjects and were not significantly different between the groups. Conclusions In summary, although reslizumab was able to blunt peripheral eosinophilia post-DEC treatment in subjects with loiasis and had no effect on microfilarial clearance, the reduction in AEC appeared to have been insufficient to prevent post-treatment AEs.

Funder

National Institute of Allergy and Infectious Diseases

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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