Vaccination Strategies: Mixing Paths Versus Matching Tracks
Achilleas Livieratos,
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Charalambos Gogos,
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Ιάσων Θωμάς
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et al.
Vaccines,
Journal Year:
2025,
Volume and Issue:
13(3), P. 308 - 308
Published: March 13, 2025
Vaccination
strategies
play
a
pivotal
role
in
achieving
broad
and
robust
immune
protection.
With
the
advent
of
new
technologies
challenges
posed
by
emerging
infectious
diseases
such
as
SARS-CoV-2,
evaluating
efficacy
homologous
(matching
tracks)
heterologous
(mixing
paths)
vaccination
regimens
is
critical.
This
article
explores
mechanistic
insights
empirical
evidence
on
benefits
limitations
these
approaches.
Language: Английский
Effectiveness of heterologous and homologous COVID-19 vaccination among immunocompromised individuals: a systematic literature review and meta-analysis
Antimicrobial Stewardship & Healthcare Epidemiology,
Journal Year:
2024,
Volume and Issue:
4(1)
Published: Jan. 1, 2024
Abstract
Objectives:
We
assessed
the
effectiveness
of
heterologous
vaccination
strategy
in
immunocompromised
individuals
regarding
COVID-19
outcomes,
comparing
it
to
homologous
approaches.
Design:
Systematic
literature
review/meta-analysis.
Methods:
searched
PubMed,
CINAHL,
EMBASE,
Cochrane
Central
Register
Controlled
Trials,
Scopus,
and
Web
Science
from
January
1,
2020
September
29,
2023.
included
studies
that
evaluated
on
through
outcomes
related
(levels
anti-SARS-CoV-2
spike
protein
IgG,
neutralizing
antibodies,
symptomatic
infection,
hospitalization,
death)
comparison
schemes.
also
used
random-effect
models
produce
pooled
odds
ratio
estimates.
Heterogeneity
was
investigated
with
I
2
estimation.
Results:
Eighteen
met
inclusion
criteria
for
this
systematic
review.
Fourteen
them
provided
quantitative
data
meta-analysis
vaccine
response,
being
four
meta-analysis.
The
strategies
(heterologous
vs
homologous)
showed
no
difference
developing
IgG
(odds
1.12
[95%
Cl:
0.73–1.72]).
Heterologous
schemes
production
antibodies
1.48
0.72–3.05])
nor
1.52
CI:
0.66–3.53]).
Conclusions:
Alternative
vaccinations
have
shown
equivalent
antibody
response
rates
schemes,
potentially
aiding
global
disparity
distribution.
Language: Английский
Homologous versus Heterologous prime-boost COVID-19 Vaccination in autologous hematopoietic stem cell transplantation recipients: a blinded randomized controlled trial
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Aug. 1, 2023
Optimizing
vaccine
efficacy
is
of
particular
concern
in
patients
undergoing
hematopoietic
stem
cell
transplantation
(HSCT),
which
mainly
have
an
inadequate
immune
response
to
primary
SARS-CoV-2
vaccination.
This
investigation
aimed
explore
the
potential
prime-boost
COVID-19
vaccination
strategies
following
autologous
(auto-)
HSCT.In
a
randomized
clinical
trial,
who
had
already
received
two
doses
receptor-binding
domain
(RBD)
tetanus
toxoid
(TT)
conjugated
during
three
nine
months
after
auto-HSCT
were
receive
either
homologous
RBD-TT
or
heterologous
inactivated
booster
dose
four
weeks
course.
The
outcome
was
comparing
anti-S
IgG
Immune
status
ratio
(ISR)
versus
dose.
assessment
safety
and
reactogenicity
adverse
events
considered
as
secondary
outcome.Sixty-one
recipients
recruited
randomly
assigned
mean
ISR
3.40
(95%
CI:
2.63-
4.16)
before
with
90.0%
seropositive
rate.
raised
5.12
4.15-
6.08)
100%
rate
(P=
0.0064)
3.42
2.67-
4.17)
93.0%
seropositivity
0.96).
In
addition,
group
suffered
more
AEs
dosage
than
group,
but
this
difference
not
statistically
significant
(p
=
0.955).
multivariable
analysis,
strategy
(heterologous
homologous),
level
dose,
length
time
between
positive
predictors
serologic
No
serious
event
attributed
vaccination.In
primed
first
year
auto-HSCT,
platform
resulted
considerably
enhanced
non-significantly
higher
strategy.
Language: Английский
Case Report: Kinetics and durability of humoral and cellular response of SARS-CoV-2 messenger RNA vaccine in a lung and kidney transplant recipient
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: July 3, 2023
We
present
a
case
report
of
63-year-old
female
health
care
worker
who
is
15
years
status
post
double
lung
transplant
and
six
living
related
donor
kidney
healthy
on
chronic
immunosuppression
regimen
including
prednisone,
mycophenolate,
tacrolimus
received
the
SARS-CoV-2
mRNA
vaccine
(Pfizer-BioNTech
BNT162b2)
primary
series
had
poor
initial
humoral
response
to
COVID-19
vaccine,
then
demonstrated
robust,
sustained
immune
against
S1
S2
antigens
for
over
seven
months
after
receiving
recommended
doses,
booster
dose,
without
developing
or
other
serious
adverse
events.
Her
vaccination
indicates
effective
formation
anti-spike
T
cell
memory
despite
immunosuppression.
This
provides
comprehensive
characterization
her
this
series.
As
effectiveness
data
updated,
as
better
understanding
hybrid
immunity
emerges,
these
findings
may
reassure
that
recipients
SOTs
be
capable
durable
responses
emerging
variants
SARS-CoV-2.
Language: Английский
Comparison of BNT162b2 and mRNA1273 vaccines in solid organ transplant recipients: Post‐Hoc analysis of a Japanese national prospective study
Scandinavian Journal of Immunology,
Journal Year:
2023,
Volume and Issue:
98(4)
Published: June 28, 2023
Abstract
The
coronavirus
disease‐19
(COVID‐19)
vaccine
efficacy
and
immunogenicity
in
the
immunocompetent
population
are
well
established.
However,
solid
organ
transplant
(SOT)
recipients,
because
of
their
use
immunosuppressive
medication,
these
severe
acute
respiratory
syndrome
2
(SARS‐CoV‐2)
vaccines
remains
suboptimal.
Both
BNT162b2
mRNA1273
have
been
used
for
some
time,
but
has
not
directly
compared
this
immunocompromised
patient
group.
We
performed
a
post‐hoc
analysis
previous
prospective
cohort
study.
inclusion
criteria
were
adult
SOT
recipients
with
active
grafts
at
least
1
month
after
SOT.
After
giving
consent,
participants
chose
to
receive
either
or
vaccine.
Anti‐spike‐protein‐S
antibody
against
SARS‐CoV‐2
was
measured.
Propensity
scores
calculated
via
logistic
regression
transform
probability
having
received
vaccine,
model
developed.
enrolled
623
recipients.
In
propensity
score‐matched
analysis,
100
selected
mRNA1273.
anti‐spike
protein
positivity
versus
3
weeks
first
dose,
second
months
6
dose
10%
19%
(
P
=
.07),
51%
58%
.30),
74%
88%
.01),
78%
87%
.13),
respectively.
conducted
comparison
as
primary
series
COVID‐19
found
significantly
better
than
BNT162b2.
Language: Английский