Heterologous prime-boost with mRNA-1273 stimulates persistent neutralising antibodies in BBIBP-CorV-vaccinated individuals
Hanisah Sharif,
No information about this author
Hazim Ghani,
No information about this author
Liyana Ahmad
No information about this author
et al.
Vaccine,
Journal Year:
2023,
Volume and Issue:
41(47), P. 6910 - 6913
Published: Oct. 24, 2023
BBIBP-CorV
inactivated
vaccine
is
one
of
the
most
prevalent
vaccines
globally,
but
immune
responses
are
far
less
studied
than
novel
COVID-19
platforms.
Longitudinal
studies
on
with
homologous
and
heterologous
booster
doses
limited.
This
study
follows
a
subset
participants
from
national
comparing
immunogenicity
levels
SARS-CoV-2
neutralising
antibody
(NAb).
Homologous
dose
significantly
increased
NAb
in
BBIBP-CorV-vaccinated
individuals.
Similar
were
observed
1
month
following
BNT162b2
or
mRNA-1273
booster.
Interestingly,
persisted
(n
=
95),
waned
at
6
9
months
50;
P
>
0.001).
The
persistence
was
also
breakthrough
infection.
provides
evidence
that
not
all
mRNA
equal
longer
term
should
provide
valuable
information
for
policy
makers
planning
programmes
vaccinated
populations.
Language: Английский
Evaluating long-term antibody responses to booster doses of COVID-19 vaccines in the Pakistani population
Shakir Hussain,
No information about this author
Fouzia Naseer,
No information about this author
Fatima Kanani
No information about this author
et al.
Pakistan Journal of Medical Sciences,
Journal Year:
2023,
Volume and Issue:
40(2(ICON))
Published: Dec. 5, 2023
Background
&
Objective:
Nearly
80
million
of
the
Pakistani
population
received
two
doses
BBIBP-CorV
vaccine,
against
SARS-CoV-2,
and
2.6
people
heterologous
booster
up
to
February
2022.
Our
objective
was
evaluate
increase
antibody
titers
in
persons
vaccinated
with
Pfizer–BioNTech
COVID-19
following
BBIBP-CorV.
Methods:
Serum
specimens
from
forty-three
participants
were
collected
4-8
weeks
at
Indus
Hospital
Health
Network,
Karachi.
A
second
set
serum
2-12
months
after
dose
administration.
Chemiluminescent
Microparticle
Immunoassay
(CMIA,
Abbott
Alinity
Quant),
pseudotyped
lentivirus
neutralization
assay
performed
on
all
specimens.
The
latter
reported
as
log
half-maximal
inhibitory
concentrations
(IC50),
calculated
using
a
nonlinear
regression
algorithm
(log
[inhibitor]
versus
normalized
response
variable
slope)
Graph
Pad
Prism
9.
paired
sample
t-test
used
ascertain
statistical
significance
difference
means
obtained
before
vaccine
doses.
Results:
Mean
log10
values
CMIA
2.90
AU/mL
3.87
respectively,
while
corresponding
IC50
through
2.45
2.80.
These
differences
statistically
significant
(p
=
<0.00001),
but
not
0.06318.).
Conclusion:
BBIBP
results
increased
total
titers,
though
neutralizing
may
start
wane
few
dose.
doi:
https://doi.org/10.12669/pjms.40.2(ICON).8951
How
cite
this:
Hussain
S,
Naseer
F,
Kanani
Aijaz
J.
Evaluating
long-term
responses
vaccines
population.
Pak
J
Med
Sci.
2024;40(2):S28-S34.
This
is
an
Open
Access
article
distributed
under
terms
Creative
Commons
Attribution
License
(http://creativecommons.org/licenses/by/3.0),
which
permits
unrestricted
use,
distribution,
reproduction
any
medium,
provided
original
work
properly
cited.
Language: Английский
Evaluation of the Diagnostic Performance of Two Automated SARS-CoV-2 Neutralization Immunoassays following Two Doses of mRNA, Adenoviral Vector, and Inactivated Whole-Virus Vaccinations in COVID-19 Naïve Subjects
Eszter Csoma,
No information about this author
Ágnes Nagy Koroknai,
No information about this author
Renáta Sütő
No information about this author
et al.
Microorganisms,
Journal Year:
2023,
Volume and Issue:
11(5), P. 1187 - 1187
Published: April 30, 2023
Background:
Limited
data
are
available
on
humoral
responses
determined
by
automated
neutralization
tests
following
the
administration
of
three
different
types
COVID-19
vaccinations.
Thus,
we
here
evaluated
anti-SARS-CoV-2
neutralizing
antibody
titers
via
two
assays
in
comparison
to
total
spike
levels.
Methods:
Healthy
participants
(n
=
150)
were
enrolled
into
subgroups
who
tested
41
(22–65)
days
after
their
second
dose
mRNA
(BNT162b2/mRNA-1273),
adenoviral
vector
(ChAdOx1/Gam-COVID-Vac)
and
inactivated
whole-virus
(BBIBP-CorV)
vaccines,
with
no
history
or
serologic
evidence
prior
SARS-CoV-2
infection.
Neutralizing
(N-Ab)
analyzed
a
Snibe
Maglumi®
800
instrument
Medcaptain
Immu
F6®
Analyzer
parallel
S
(S-Ab)
levels
(Roche
Elecsys®
e602).
Results:
Subjects
administered
vaccines
demonstrated
significantly
higher
N-Ab
S-Ab
compared
those
received
vaccinations
(p
<
0.0001).
methods
correlated
each
other
(r
0.9608;
p
0.0001)
0.9432
r
0.9324;
0.0001,
respectively).
Based
values,
new
optimal
threshold
Roche
was
calculated
(166
BAU/mL)
for
discrimination
seropositivity
showing
an
AUC
value
0.975
Low
post-vaccination
(median
0.25
μg/mL
7.28
AU/mL)
measured
8)
infected
within
6
months
immunizations.
Conclusion:
Both
effective
evaluate
various
Language: Английский