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  1. AU="Hana M El Sahly"
  2. AU="Tasnim, S."
  3. AU="Crundwell, David J"
  4. AU="Pavan, William J"
  5. AU="Kanie, Keitaro"
  6. AU="Li, Huling"
  7. AU="Joeres, Roman"
  8. AU="Lynce, Ana"
  9. AU="Goksu, Muhammed M"
  10. AU="Škvor, Jiří"
  11. AU=Fomenko Ekaterina Vladimirovna
  12. AU=Abootalebi Shahram AU=Abootalebi Shahram
  13. AU="Salim Kabbani, Mohamed"
  14. AU="Mrówka, Ryszard"
  15. AU="Guzman-Esquivel, José"
  16. AU="Shamloul, Sara"
  17. AU="Fazzari, Carmine"
  18. AU="Tang, K B"
  19. AU="Sansbury, Brian E"
  20. AU="Chapuy-Regaud, Sabine"
  21. AU="Y.Yang, " AU="Y.Yang, "
  22. AU="Banu Bozkurt"
  23. AU="Aguib, Yasmine"

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  1. Artikel ; Online: A randomized, controlled Phase 1b trial of the Sm-TSP-2 Vaccine for intestinal schistosomiasis in healthy Brazilian adults living in an endemic area.

    David J Diemert / Rodrigo Correa-Oliveira / Carlo Geraldo Fraga / Frederico Talles / Marcella Rezende Silva / Shital M Patel / Shirley Galbiati / Jessie K Kennedy / Jordan S Lundeen / Maria Flavia Gazzinelli / Guangzhao Li / Lara Hoeweler / Gregory A Deye / Maria Elena Bottazzi / Peter J Hotez / Hana M El Sahly / Wendy A Keitel / Jeffrey Bethony / Robert L Atmar

    PLoS Neglected Tropical Diseases, Vol 17, Iss 3, p e

    2023  Band 0011236

    Abstract: Background Recombinant Schistosoma mansoni Tetraspanin-2 formulated on Alhydrogel (Sm-TSP-2/Alhydrogel) is being developed to prevent intestinal and hepatic disease caused by S. mansoni. The tegumentary Sm-TSP-2 antigen was selected based on its unique ... ...

    Abstract Background Recombinant Schistosoma mansoni Tetraspanin-2 formulated on Alhydrogel (Sm-TSP-2/Alhydrogel) is being developed to prevent intestinal and hepatic disease caused by S. mansoni. The tegumentary Sm-TSP-2 antigen was selected based on its unique recognition by cytophilic antibodies in putatively immune individuals living in areas of ongoing S. mansoni transmission in Brazil, and preclinical studies in which vaccination with Sm-TSP-2 protected mice following infection challenge. Methods A randomized, observer-blind, controlled, Phase 1b clinical trial was conducted in 60 healthy adults living in a region of Brazil with ongoing S. mansoni transmission. In each cohort of 20 participants, 16 were randomized to receive one of two formulations of Sm-TSP-2 vaccine (adjuvanted with Alhydrogel only, or with Alhydrogel plus the Toll-like receptor-4 agonist, AP 10-701), and 4 to receive Euvax B hepatitis B vaccine. Successively higher doses of antigen (10 μg, 30 μg, and 100 μg) were administered in a dose-escalation fashion, with progression to the next dose cohort being dependent upon evaluation of 7-day safety data after all participants in the preceding cohort had received their first dose of vaccine. Each participant received 3 intramuscular injections of study product at intervals of 2 months and was followed for 12 months after the third vaccination. IgG and IgG subclass antibody responses to Sm-TSP-2 were measured by qualified indirect ELISAs at pre- and post-vaccination time points through the final study visit. Results Sm-TSP-2/Alhydrogel administered with or without AP 10-701 was well-tolerated in this population. The most common solicited adverse events were mild injection site tenderness and pain, and mild headache. No vaccine-related serious adverse events or adverse events of special interest were observed. Groups administered Sm-TSP-2/Alhydrogel with AP 10-701 had higher post-vaccination levels of antigen-specific IgG antibody. A significant dose-response relationship was seen in those administered ...
    Schlagwörter Arctic medicine. Tropical medicine ; RC955-962 ; Public aspects of medicine ; RA1-1270
    Thema/Rubrik (Code) 610
    Sprache Englisch
    Erscheinungsdatum 2023-03-01T00:00:00Z
    Verlag Public Library of Science (PLoS)
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  2. Artikel: Stable emulsion (SE) alone is an effective adjuvant for a recombinant, baculovirus-expressed H5 influenza vaccine in healthy adults: A Phase 2 trial

    Treanor, John J / Brandon Essink / Derek Muse / Hana M. El Sahly / Karen L. Goldenthal / Laurence Chu / Lisa M. Dunkle / Peter Patriarca / Ruvim Izikson

    Vaccine. 2017 Feb. 07, v. 35, no. 6

    2017  

    Abstract: Influenza A viruses of the H5 subtype have been identified as important targets for development of vaccines. Achievement of potentially protective antibody responses against pandemic strains has usually required the use of adjuvants.We evaluated a ... ...

    Abstract Influenza A viruses of the H5 subtype have been identified as important targets for development of vaccines. Achievement of potentially protective antibody responses against pandemic strains has usually required the use of adjuvants.We evaluated a candidate A/Indonesia/05/2005 (H5) vaccine generated by baculovirus expression of recombinant hemagglutinin (HA) protein with or without stable emulsion (SE) as an adjuvant.Healthy subjects 18–49years old were randomized (1:1:1:1) to receive two doses of rHA at 7.5ug per dose (no adjuvant), or 3.8ug, 7.5ug, or 15ug per dose formulated with 2% SE separated by 21days, and serum from day 0, 21, 42, and 201 assessed by hemagglutination-inhibition.341 subjects were enrolled in the study and 321 received two doses of vaccine. Vaccination was well tolerated in all groups. After two doses, seroconversion was noted in only 9% (95% confidence interval 4%, 17%) of recipients of unadjuvanted vaccine at 7.5ug, but in 70% (59%, 80%), 76% (65%, 85%), and 83% (73%, 91%) of those receiving adjuvanted vaccine at 3.8ug, 7.5ug, or 15ug respectively.Stable emulsion alone is an effective adjuvant for rH5 vaccine in healthy adults. All three adjuvanted dose groups met the current criterion for seroconversion rate for pandemic vaccines. This dose-ranging study also identified a group (15ug per dose formulated with 2% SE) that met the criteria for both seroconversion and percentage of subjects achieving an HI antibody titer⩾40. These Phase 2 data support the further clinical development of SE adjuvanted Panblok H5.Clinical trial registration: NCT01612000.The protocol was approved by the relevant Institutional Review Board for each study site, and the study was conducted in accordance with the Declaration of Helsinki, International Conference of Harmonisation – Good Clinical Practice, and all applicable laws and regulations. All participants provided written informed consent before study procedures.
    Schlagwörter adjuvants ; adults ; antibodies ; blood serum ; confidence interval ; emulsions ; hemagglutinins ; influenza ; Influenza A virus ; laws and regulations ; pandemic ; seroconversion ; vaccination ; vaccine development ; vaccines
    Sprache Englisch
    Erscheinungsverlauf 2017-0207
    Umfang p. 923-928.
    Erscheinungsort Elsevier Ltd
    Dokumenttyp Artikel
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2016.12.053
    Datenquelle NAL Katalog (AGRICOLA)

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  3. Artikel: Immunogenicity and safety of four different dosing regimens of anthrax vaccine adsorbed for post-exposure prophylaxis for anthrax in adults

    Bernstein, David I / Hana M. El Sahly / Heather Hill / Johannes B. Goll / Lisa Jackson / Nadine Rouphael / Paul Spearman / Shital M. Patel / Thomas L. Rudge

    Elsevier Ltd Vaccine. 2014 Oct. 29, v. 32, no. 47

    2014  

    Abstract: Strategies to implement post exposure prophylaxis (PEP) in case of an anthrax bioterror event are needed. To increase the number of doses of vaccine available we evaluated reducing the amount of vaccine administered at each of the vaccinations, and ... ...

    Abstract Strategies to implement post exposure prophylaxis (PEP) in case of an anthrax bioterror event are needed. To increase the number of doses of vaccine available we evaluated reducing the amount of vaccine administered at each of the vaccinations, and reducing the number of doses administered.Healthy male and non-pregnant female subjects between the ages of 18 and 65 were enrolled and randomized 1:1:1:1 to one of four study arms to receive 0.5mL (standard dose) of vaccine subcutaneously (SQ) at: (A) days 0, 14; (B) days 0 and 28; (C) days 0, 14, and 28; or (D) 0.25mL at days 0, 14, and 28. A booster was provided on day 180. Safety was assessed after each dose. Blood was obtained on days 0, 7, 14, 21, 28, 35, 42, 49, 56, 63, 70, 84, 100, 180, and 201 and both Toxin Neutralizing antibody and anti-PA IgG antibody measured.Almost all subjects developed some local reactions with 46–64% reported to be of moderate severity and 3.3% severe during the primary series. Vaccine groups that included a day 14 dose induced a ≥4 fold antibody rise in more subjects on days 21, 28, and 35 than the arm without a day 14 dose. However, schedules with a full day 28 dose induced higher peak levels of antibody that persisted longer. The half dose regimen did not induce antibody as well as the full dose study arms.Depending on the extent of the outbreak, effectiveness of antibiotics and availability of vaccine, the full dose 0, 28 or 0, 14, 28 schedules may have advantages.
    Schlagwörter adults ; anthrax ; antibiotics ; blood ; disease control ; females ; immune response ; immunoglobulin G ; males ; neutralization ; neutralizing antibodies ; vaccination ; vaccines
    Sprache Englisch
    Erscheinungsverlauf 2014-1029
    Umfang p. 6284-6293.
    Erscheinungsort Elsevier Ltd
    Dokumenttyp Artikel
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2014.08.076
    Datenquelle NAL Katalog (AGRICOLA)

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  4. Artikel: Safety and immunogenicity of a modified vaccinia Ankara vaccine using three immunization schedules and two modes of delivery: A randomized clinical non-inferiority trial

    Jackson, Lisa A / Colin Fields / Edwin L. Anderson / Evan J. Anderson / Hana M. El Sahly / Heather Hill / Irene Graham / James D. Campbell / Johannes B. Goll / Karen L. Kotloff / Mark J. Mulligan / Nadine Rouphael / Patricia L. Winokur / Robert L. Atmar / Sharon E. Frey / Shital M. Patel / Wendy Keitel

    Vaccine. 2017 Mar. 23, v. 35, no. 13

    2017  

    Abstract: To guide the use of modified vaccinia Ankara (MVA) vaccine in response to a release of smallpox virus, the immunogenicity and safety of shorter vaccination intervals, and administration by jet injector (JI), were compared to the standard schedule of ... ...

    Abstract To guide the use of modified vaccinia Ankara (MVA) vaccine in response to a release of smallpox virus, the immunogenicity and safety of shorter vaccination intervals, and administration by jet injector (JI), were compared to the standard schedule of administration on Days 1 and 29 by syringe and needle (S&N).Healthy adults 18–40years of age were randomly assigned to receive MVA vaccine subcutaneously by S&N on Days 1 and 29 (standard), Days 1 and 15, or Days 1 and 22, or to receive the vaccine subcutaneously by JI on Days 1 and 29. Blood was collected at four time points after the second vaccination for plaque reduction neutralization test (PRNT) (primary endpoint) and ELISA (secondary endpoint) antibody assays. For each subject, the peak PRNT (or ELISA) titer was defined by the highest PRNT (or ELISA) titer among all available measurements post second vaccination. Non-inferiority of a non-standard arm compared to the standard arm was met if the upper limit of the 98.33% confidence interval of the difference in the mean log2 peak titers between the standard and non-standard arm was less than 1.Non-inferiority of the PRNT antibody response was not established for any of the three non-standard study arms. Non-inferiority of the ELISA antibody response was established for the Day 1 and 22 compressed schedule and for administration by JI. Solicited local reactions, such as redness and swelling, tended to be more commonly reported with JI administration. Four post-vaccination hypersensitivity reactions were observed.Evaluations of the primary endpoint of PRNT antibody responses do not support alternative strategies of administering MVA vaccine by S&N on compressed schedules or administration by JI on the standard schedule.Trial Registration: clinicaltrials.gov Identifier: NCT01827371.
    Schlagwörter adults ; antibodies ; blood ; confidence interval ; enzyme-linked immunosorbent assay ; hypersensitivity ; immune response ; neutralization tests ; vaccination ; vaccines ; Variola virus
    Sprache Englisch
    Erscheinungsverlauf 2017-0323
    Umfang p. 1675-1682.
    Erscheinungsort Elsevier Ltd
    Dokumenttyp Artikel
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2017.02.032
    Datenquelle NAL Katalog (AGRICOLA)

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  5. Artikel: Tularemia vaccine: Safety, reactogenicity, “Take” skin reactions, and antibody responses following vaccination with a new lot of the Francisella tularensis live vaccine strain – A phase 2 randomized clinical Trial

    Mulligan, Mark J / Allison Beck / Edwin Anderson / Hana M. El Sahly / Heather Hill / Irene Graham / Jack T. Stapleton / Johannes B. Goll / Marcela F. Pasetti / Marcelo B. Sztein / Nadine Rouphael / Patricia L. Winokur / Robert L. Atmar / Samer S. El-Kamary / Sharon E. Frey / Shital M. Patel / Srilatha Edupuganti / Wendy A. Keitel / Wilbur H. Chen

    Vaccine. 2017 Aug. 24, v. 35, no. 36

    2017  

    Abstract: Tularemia is caused by Francisella tularensis, a gram-negative bacterium that has been weaponized as an aerosol. For protection of personnel conducting biodefense research, the United States Army required clinical evaluation of a new lot of tularemia ... ...

    Abstract Tularemia is caused by Francisella tularensis, a gram-negative bacterium that has been weaponized as an aerosol. For protection of personnel conducting biodefense research, the United States Army required clinical evaluation of a new lot of tularemia live vaccine strain manufactured in accordance with Current Good Manufacturing Practices.A phase 2 randomized clinical trial compared the new lot (DVC-LVS) to the existing vaccine that has been in use for decades (USAMRIID-LVS). The vaccines were delivered by scarification to 228 participants. Safety, reactogenicity, take and/or antibody levels were assessed on days 0, 1, 2, 8, 14, 28, 56, and 180.Both vaccines were safe and had acceptable reactogenicity profiles during six months of follow-up. There were no serious or grade 3 and 4 laboratory adverse events. Moderate systemic reactogenicity (mostly headache or feeling tired) was reported by ∼23% of participants receiving either vaccine. Injection site reactogenicity was mostly mild itchiness and pain. The frequencies of vaccine take skin reactions were 73% (95% CI, 64, 81) for DVC-LVS and 80% (95% CI, 71, 87) for USAMRIID-LVS. The 90% CI for the difference in proportions was −6.9% (−16.4, 2.6). The rates of seroconversion measured by microagglutination assay on days 28 or 56 were 94% (95% CI, 88, 98; n=98/104) for DVC-LVS and 94% (95% CI, 87, 97; n=103/110) for USAMRIID-LVS (p=1.00). Day 14 sera revealed more rapid seroconversion for DVC-LVS relative to USAMRIID-LVS: 82% (95% CI, 73, 89) versus 55% (95% CI, 45, 65), respectively (p<0.0001).The DVC-LVS vaccine had similar safety, reactogenicity, take and antibody responses compared to the older USAMRIID vaccine, and was superior for early (day 14) antibody production. Vaccination take was not a sensitive surrogate for seroconversion in a multi-center study where personnel at five research clinics performed assessments.ClinicalTrials.gov identifier NCT01150695
    Schlagwörter aerosols ; antibodies ; antibody formation ; clinical examination ; clinical trials ; Francisella tularensis ; Gram-negative bacteria ; headache ; human resources ; injection site ; live vaccines ; manufacturing ; seroconversion ; tularemia ; vaccination ; United States
    Sprache Englisch
    Erscheinungsverlauf 2017-0824
    Umfang p. 4730-4737.
    Erscheinungsort Elsevier Ltd
    Dokumenttyp Artikel
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2017.07.024
    Datenquelle NAL Katalog (AGRICOLA)

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