TY - JOUR
T1 - Optimising the timing of whooping cough immunisation in mums (OpTIMUM) through investigating pertussis vaccination in pregnancy
T2 - an open-label, equivalence, randomised controlled trial
AU - OpTIMUM Study Group
AU - Calvert, Anna
AU - Amirthalingam, Gayatri
AU - Andrews, Nick
AU - Basude, Sneha
AU - Coleman, Matthew
AU - Cuthbertson, Hannah
AU - England, Anna
AU - Greening, Vanessa
AU - Hallis, Bassam
AU - Johnstone, Edward
AU - Jones, Christine E.
AU - Karampatsas, Konstantinos
AU - Khalil, Asma
AU - Le Doare, Kirsty
AU - Matheson, Mary
AU - Peregrine, Elisabeth
AU - Snape, Matthew D.
AU - Vatish, Manu
AU - Heath, Paul T.
AU - Burtt, Agnieszka
AU - Byrne, Wendy
AU - Capp, Angelika
AU - Carty, Lotoyah
AU - Chawla, Krina
AU - Collins, Sarah
AU - Cornish, Emily
AU - Daniel, Olwenn
AU - Fretwell, Jessica
AU - Gorringe, Andrew
AU - Gubbins, Teresa
AU - Hall, Tom
AU - Johnston, Susan
AU - Khan, Uzma
AU - Lim, Suzy
AU - Martin, Nicki
AU - Morey, Ella
AU - Mossop, Jude
AU - O'Brien, Katie
AU - Owino, Nelly
AU - Powell, Deborah
AU - Ramkhelawon, Laxmee
AU - Ratcliffe, Helen
AU - Roberts, Hannah
AU - Roseman, Fenella
AU - Sparks, Laura
AU - Stapley, Lorraine
AU - Taylor, Stephen
AU - Walbridge, Fiona
AU - Watts, Rosie
AU - Wellstead, Susan J.
N1 - Publisher Copyright:
© 2023 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2023/5
Y1 - 2023/5
N2 - Background: Pertussis vaccination in pregnancy is recommended in many countries to provide protection to young infants. The best timing for this vaccination is uncertain. In the UK, vaccination is recommended between 16 weeks and 32 weeks of gestation. In this trial we aimed to investigate the equivalence of three time periods for pertussis vaccination in pregnancy. Methods: In this open-label, equivalence, randomised controlled trial to investigate equivalence of different time windows for pertussis vaccination in pregnancy, participants were randomly assigned (1:1:1 ratio) to receive a pertussis-containing vaccine (Boostrix-inactivated poliovirus vaccine) in one of three gestational age groups, comprising group 1 (≤23 weeks + 6 days), group 2 (24–27 weeks + 6 days), and group 3 (28–31 weeks + 6 days) using a computer-generated randomisation list. The primary outcome was concentration of pertussis-specific antibodies in the infant born at term at birth. Maternal blood sampling was done before and 2 weeks after vaccination and at delivery, together with a cord sample, and an infant sample was collected at least 4 weeks after primary vaccination. Reactogenicity was assessed for 7 days after vaccination. This trial was registered with ClinicalTrials.gov (NCT03908164). Findings: Between May 7, 2019, and Feb 13, 2020, of 1010 women assessed for eligibility, 364 women were recruited and 351 received the intervention (120 in group 1, 119 in group 2, and 112 in group 3). Equivalence of time periods was demonstrated for anti-pertussis toxin and anti-pertactin IgG concentrations. The cord blood geometric mean concentrations of anti-filamentous haemagglutinin IgG were higher with increasing gestational age at vaccination, such that for infants in group 1 (≤23 weeks + 6 days), equivalence to group 3 (28–31 weeks + 6 days) was not shown. Reported rates of fever were similar between study groups. Interpretation: Pertussis vaccination at three different time intervals in pregnancy resulted in equivalent concentrations of IgG antibodies in infants against two of the three pertussis antigens assessed. Overall, these findings support recommendations to vaccinate any time between 16 weeks and 32 weeks of gestation. Funding: The Thrasher Research Fund and the National Immunisation Schedule Evaluation Consortium through the National Institute for Health and Care Research policy research programme.
AB - Background: Pertussis vaccination in pregnancy is recommended in many countries to provide protection to young infants. The best timing for this vaccination is uncertain. In the UK, vaccination is recommended between 16 weeks and 32 weeks of gestation. In this trial we aimed to investigate the equivalence of three time periods for pertussis vaccination in pregnancy. Methods: In this open-label, equivalence, randomised controlled trial to investigate equivalence of different time windows for pertussis vaccination in pregnancy, participants were randomly assigned (1:1:1 ratio) to receive a pertussis-containing vaccine (Boostrix-inactivated poliovirus vaccine) in one of three gestational age groups, comprising group 1 (≤23 weeks + 6 days), group 2 (24–27 weeks + 6 days), and group 3 (28–31 weeks + 6 days) using a computer-generated randomisation list. The primary outcome was concentration of pertussis-specific antibodies in the infant born at term at birth. Maternal blood sampling was done before and 2 weeks after vaccination and at delivery, together with a cord sample, and an infant sample was collected at least 4 weeks after primary vaccination. Reactogenicity was assessed for 7 days after vaccination. This trial was registered with ClinicalTrials.gov (NCT03908164). Findings: Between May 7, 2019, and Feb 13, 2020, of 1010 women assessed for eligibility, 364 women were recruited and 351 received the intervention (120 in group 1, 119 in group 2, and 112 in group 3). Equivalence of time periods was demonstrated for anti-pertussis toxin and anti-pertactin IgG concentrations. The cord blood geometric mean concentrations of anti-filamentous haemagglutinin IgG were higher with increasing gestational age at vaccination, such that for infants in group 1 (≤23 weeks + 6 days), equivalence to group 3 (28–31 weeks + 6 days) was not shown. Reported rates of fever were similar between study groups. Interpretation: Pertussis vaccination at three different time intervals in pregnancy resulted in equivalent concentrations of IgG antibodies in infants against two of the three pertussis antigens assessed. Overall, these findings support recommendations to vaccinate any time between 16 weeks and 32 weeks of gestation. Funding: The Thrasher Research Fund and the National Immunisation Schedule Evaluation Consortium through the National Institute for Health and Care Research policy research programme.
UR - http://www.scopus.com/inward/record.url?scp=85154617468&partnerID=8YFLogxK
U2 - 10.1016/S2666-5247(22)00332-9
DO - 10.1016/S2666-5247(22)00332-9
M3 - Article
AN - SCOPUS:85154617468
SN - 2666-5247
VL - 4
SP - e300-e308
JO - The Lancet Microbe
JF - The Lancet Microbe
IS - 5
ER -