Validation and Clinical Performance of a Non-Commercial ELISA for SARS-CoV-2 Anti-RBD IgA Antibodies
Sheila Chávez-Valdés,
Ana K Marichal-Rodríguez,
Yahima Chacón-Quintero
и другие.
Analytical Biochemistry,
Год журнала:
2025,
Номер
700, С. 115787 - 115787
Опубликована: Янв. 31, 2025
Язык: Английский
The single-dose Janssen Ad26.COV2.S COVID-19 vaccine elicited robust and persistent anti-spike IgG antibody responses in a 12-month Ugandan cohort
Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Май 8, 2024
Introduction
The
study
investigation
examined
the
immune
response
to
Janssen
Ad26.COV2.S
COVID-19
vaccine
within
a
Ugandan
cohort,
specifically
targeting
antibodies
directed
against
spike
(S)
and
nucleocapsid
(N)
proteins.
We
aimed
examine
durability
robustness
of
induced
antibody
while
also
assessing
occurrences
breakthrough
infections
previous
anti-Spike
seropositivity
SARS-CoV-2.
Methods
included
319
specimens
collected
over
12
months
from
60
vaccinees
aged
18
64.
Binding
were
quantified
using
validated
ELISA
method
measure
SARS-CoV-2-specific
IgG,
IgM,
IgA
levels
S
N
Results
results
showed
that
baseline
for
S-IgG
was
high
at
67%,
increasing
98%
by
day
14
consistently
stayed
above
95%
up
months.
However,
S-IgM
responses
remained
suboptimal.
A
raised
S-IgA
rate
seen
doubled
40%
86%
just
two
weeks
following
initial
dose,
indicating
sustained
robust
peripheral
immunity.
An
increase
in
N-IgG
nine
post-vaccination
suggested
eight
cases.
Baseline
cross-reactivity
influenced
spike-directed
responses,
with
individuals
harbouring
showing
notably
higher
responses.
Discussion
Robust
long
lasting
infection-induced
observed,
significant
implications
regions
where
administering
subsequent
doses
poses
logistical
challenges.
Язык: Английский
mRNA Vaccines Against COVID-19 as Trailblazers for Other Human Infectious Diseases
Vaccines,
Год журнала:
2024,
Номер
12(12), С. 1418 - 1418
Опубликована: Дек. 16, 2024
mRNA
vaccines
represent
a
milestone
in
the
history
of
vaccinology,
because
they
are
safe,
very
effective,
quick
and
cost-effective
to
produce,
easy
adapt
should
antigen
vary,
able
induce
humoral
cellular
immunity.
Methods:
To
date,
only
two
COVID-19
one
RSV
have
been
approved.
However,
several
currently
under
development
for
prevention
human
viral
(influenza,
immunodeficiency
virus
[HIV],
Epstein–Barr
virus,
cytomegalovirus,
Zika,
respiratory
syncytial
metapneumovirus/parainfluenza
3,
Chikungunya,
Nipah,
rabies,
varicella
zoster
herpes
simplex
1
2),
bacterial
(tuberculosis),
parasitic
(malaria)
diseases.
Results:
RNA
viruses,
such
as
severe
acute
syndrome
coronavirus
(SARS-CoV)-2,
HIV,
influenza,
characterized
by
high
variability,
thus
creating
need
rapidly
circulating
strain,
task
that
can
easily
accomplish;
however,
speed
variability
may
be
higher
than
time
needed
vaccine
adapted.
vaccines,
using
lipid
nanoparticles
delivery
system,
act
adjuvants,
powerfully
stimulating
innate
well
adaptive
immunity,
both
humoral,
which
is
waning,
cell-mediated,
highly
persistent.
Safety
profiles
were
satisfactory,
considering
slight
increase
prognostically
favorable
anaphylactic
reactions
young
females
myopericarditis
males
has
observed.
Conclusions:
The
pandemic
determined
shift
use
RNA:
after
having
used
medicine
micro-RNAs
tumor
new
era
anti-infectious
begun,
great
development,
either
improve
already
available,
but
unsatisfactory,
or
develop
protective
against
infectious
agents
no
preventative
tools
realized
yet.
Язык: Английский