Medicina,
Journal Year:
2024,
Volume and Issue:
60(12), P. 2071 - 2071
Published: Dec. 16, 2024
Background
and
Objectives:
Coinfection
with
SARS-CoV-2
extrapulmonary
tuberculosis
(extraPTB)
presents
unique
clinical
challenges
due
to
dual
inflammatory
responses
potential
differences
in
patient
profiles
compared
those
infection
alone.
This
study
uniquely
contributes
the
underexplored
interaction
between
extraPTB
SARS-CoV-2,
focusing
on
systemic
inflammation
as
a
critical
determinant
of
outcomes.
Materials
Methods:
retrospective,
cross-sectional
included
123
patients
aged
19–91
years,
hospitalized
at
Victor
Babeș
Hospital
Timișoara
from
March
2020
2022.
We
23
coinfected
100
age-matched
SARS-CoV-2-only
patients.
Clinical
records
were
examined
for
demographic,
clinical,
laboratory
data.
Results:
The
group
was
younger,
65%
under
40
presented
significantly
higher
IL-6,
PCT,
transaminase
levels.
Coexisting
COPD
type
2
diabetes
independent
predictors
coinfection.
A
SpO2
diagnosis
positively
associated
coinfection
likelihood
(OR
=
5.37),
while
CT
scores
indicated
less
pulmonary
involvement
Non-fatal
outcomes
more
frequent
(95.7%
sensitivity),
only
one
had
fatal
outcome
versus
17
group.
Low
elevated
IL-6
significant
mortality,
severe
symptoms
tripling
fatality
odds.
Conclusions:
is
younger
age,
heightened
inflammation,
longer
hospital
stays
but
does
not
increase
mortality
risk
These
findings
underscore
importance
monitoring
markers
developing
tailored
management
strategies
improve
long-term
care
patients,
especially
resource-limited
settings.
Journal of Clinical Medicine,
Journal Year:
2025,
Volume and Issue:
14(8), P. 2782 - 2782
Published: April 17, 2025
Background:
Tuberculosis
and
COVID-19
co-infection
poses
significant
clinical
challenges,
with
pulmonary
TB
(PTB)
extrapulmonary
(extraPTB)
potentially
influencing
disease
progression
outcomes
differently.
This
study
aims
to
compare
the
manifestations,
inflammatory
markers,
between
PTB
extraPTB
patients
SARS-CoV-2
co-infection.
Methods:
A
retrospective,
cross-sectional
was
conducted
on
55
hospitalized
adults
TB-COVID-19
from
March
2020
2022.
Patients
were
divided
into
(n
=
32)
23)
groups.
Demographic,
clinical,
laboratory,
imaging
data
collected
analyzed
using
statistical
models,
including
ANCOVA,
LASSO
regression,
Random
Forest
classification,
identify
key
predictors
of
hospitalization
duration
mortality.
Results:
had
significantly
lower
BMI,
worse
oxygenation
status,
greater
lung
involvement
CT
compared
patients.
CRP
elevated
in
PTB,
while
IL-6
levels
higher
extraPTB.
Hospitalization
primarily
influenced
by
coagulation
markers
(IL-6,
D-dimer,
neutrophil
count,
systemic
index),
BMI
associated
shorter
stays.
Mortality
risk
strongly
correlated
impairment
(worst
SpO2,
SpO2
at
diagnosis),
burden
(CRP,
LDH),
severity
score,
rather
than
localization.
Conclusions:
localization
did
not
independently
affect
or
mortality
risk.
Instead,
severe
involvement,
inflammation,
hypoxemia
strongest
poor
outcomes.
These
findings
emphasize
importance
early
stratification
based
respiratory
optimize
patient
management.
Further
research
is
needed
clarify
long-term
impact
co-infection,
particularly
cases.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: March 21, 2024
With
the
increasing
number
of
people
worldwide
infected
with
SARS-CoV-2,
likelihood
co-infection
and/or
comorbidities
is
rising.
The
impact
these
co-infections
on
patient's
immune
system
remains
unclear.
This
study
aims
to
investigate
immunological
characteristics
secondary
infections
in
hospitalized
COVID-19
patients,
and
preliminarily
predict
potential
therapeutic
effects
traditional
Chinese
medicine
their
derivatives
for
treatment
co-infections.
In
this
retrospective
cohort
study,
we
included
131
patients
laboratory-confirmed
COVID-19,
whom
there
were
64
mild
67
severe
cases.
We
analyzed
clinical
immunologic
data,
including
circulating
cell
numbers,
levels
inflammatory
factors
viral
load,
comparing
without
co-infection.
Among
41
(31.3%)
positive,
33
(80.5%)
having
disease
14
(34.1%)
them
resulting
fatalities.
Co-infected
exhibited
significantly
higher
severity
mortality
rates
compared
non-co-infected
counterparts.
had
lower
absolute
counts
lymphocytes,
total
T
CD4+
cells,
CD8+
cells
B
while
hs-CRP,
PCT
IL-6
elevated
patients.
Additionally,
load
co-infected
was
than
Co-infection
emerges
as
a
dangerous
factor
elevating
risk
pneumonia
mortality.
suppresses
host's
response
by
reducing
lymphocytes
inflammation,
thereby
diminishing
antiviral
anti-infective
system,
which
promotes
disease.
Therefore,
it
crucial
implement
infection
prevention
measures
minimize
spread
among
changes
biomarkers
provide
theoretical
basis
effective
medicine.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 27, 2024
SARS-CoV-2
infection
leads
to
vastly
divergent
clinical
outcomes
ranging
from
asymptomatic
fatal
disease.
Co-morbidities,
sex,
age,
host
genetics
and
vaccine
status
are
known
affect
disease
severity.
Yet,
how
the
inflammatory
milieu
of
lung
at
time
exposure
impacts
control
viral
replication
remains
poorly
understood.
We
demonstrate
here
that
immune
events
in
mouse
closely
preceding
significantly
impact
we
identify
key
innate
pathways
required
limit
replication.
A
diverse
set
pulmonary
stimuli,
including
resolved
antecedent
respiratory
infections
with
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: June 20, 2024
At
the
beginning
of
COVID-19
pandemic
those
with
underlying
chronic
lung
conditions,
including
tuberculosis
(TB),
were
hypothesized
to
be
at
higher
risk
severe
disease.
However,
there
is
inconclusive
clinical
and
preclinical
data
confirm
specific
SARS-CoV-2
poses
for
millions
individuals
infected
Mycobacterium
(M.tb).
We
others
have
found
that
compared
singly
mice,
mice
co-infected
M.tb
leads
reduced
severity
alone.
Consequently,
a
large
interest
in
identifying
molecular
mechanisms
responsible
infection
observed
co-infection.
To
address
this,
we
conducted
comprehensive
characterization
co-infection
model
performed
mechanistic
vitro
modeling
dynamically
assess
how
innate
immune
response
induced
by
restricts
viral
replication.
Our
study
has
successfully
identified
several
cytokines
induce
upregulation
anti-viral
genes
epithelial
cells,
thereby
providing
protection
prior
challenge
SARS-CoV-2.
In
conclusion,
our
offers
understanding
key
pathways
an
existing
bacterial
effectively
activity
identifies
candidate
therapeutic
targets
infection.
Science Immunology,
Journal Year:
2024,
Volume and Issue:
9(102)
Published: Dec. 6, 2024
Severity
of
COVID-19
is
affected
by
multiple
factors;
however,
it
not
understood
how
the
inflammatory
milieu
lung
at
time
SARS-CoV-2
exposure
affects
control
viral
replication.
Here,
we
demonstrate
that
immune
events
in
mouse
closely
preceding
infection
affect
and
identify
innate
pathways
limit
Pulmonary
stimuli
including
resolved,
antecedent
respiratory
infections
with
Staphylococcus
aureus
or
influenza,
ongoing
pulmonary
Mycobacterium
tuberculosis
infection,
ovalbumin/alum-induced
asthma,
airway
administration
TLR
ligands
recombinant
cytokines
all
establish
an
antiviral
state
restricts
In
addition
to
type
I
interferons,
TNFα
IL-1
potently
precondition
for
enhanced
control.
Our
work
shows
may
benefit
from
immunologically
quiescent
microenvironment
suggests
heterogeneity
inflammation
contribute
variability
disease
outcomes.
Pediatric Pulmonology,
Journal Year:
2024,
Volume and Issue:
59(12), P. 3446 - 3456
Published: Aug. 26, 2024
Abstract
Introduction
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS‐CoV‐2)
pandemic
had
a
significant
impact
on
tuberculosis
(TB)
control
globally,
with
the
number
of
new
TB
diagnoses
decreasing.
Coinfection
some
viruses,
especially
measles,
could
aggravate
in
children.
This
is
presumably
result
depressed
cellular
immunity.
Reports
children
and
SARS‐CoV‐2
coinfection
are
limited.
Methods
A
retrospective
analysis
up
to
13
years
old
admitted
Tygerberg
Hospital,
Cape
Town,
South
Africa,
from
March
2020
December
2022
suspected
TB‐induced
airway
compression
requiring
bronchoscopy.
Children
were
included
if
they
presented
intrathoracic
obstruction
and/or
radiographic
evidence
complicated
TB.
patients
divided
into
two
groups
based
polymerase
chain
reaction
results.
Demographics,
exposure,
microbiology,
laboratory
data,
imaging,
inflammatory
cytokine
levels,
bronchoscopy
data
collected.
Statistical
analyses
compared
positive
negative
groups.
Results
Of
50
undergoing
for
obstruction,
7
(14%)
positive.
Cough
was
more
prevalent
group
(
p
=
0.04).
There
no
difference
culture
yield
between
However,
showed
slower
radiological
improvement
at
1
month
0.01),
pleural
effusions
<
0.001),
higher
need
endoscopic
enucleation
0.001).
FDG
PET/CT
scans
indicated
an
ongoing
inflammation
group.
Conclusions
appears
complicate
disease
course,
necessitating
medical
interventions
demonstrating
longer
duration
process.
Further
research
needed
understand
viral
infections
progression
outcomes
pediatric
patients.
Contribuciones a las Ciencias Sociales,
Journal Year:
2024,
Volume and Issue:
17(1), P. 8242 - 8255
Published: Jan. 31, 2024
A
Covid-19
é
uma
doença
infecciosa
altamente
contagiosa
e
potencialmente
perigosa
que
pode
ser
assintomática
ou
sintomática,
a
depender
da
resposta
imunológica
do
hospedeiro
contra
o
SARS-CoV-2.
Paralelamente,
tuberculose
continua
como
um
problema
de
saúde
pública
negligenciado
também
apresenta
alta
morbimortalidade,
caso
não
seja
tratada
adequadamente.
Ainda
há
muito
explorado
sobre
coinfecção
com
ambas
as
doenças,
por
isso
este
artigo
explorou
os
principais
aspectos
biológicos
clínicos
Covid-19,
visto
são
informações
essenciais
para
compreensão
adoção
medidas
prevenção
controle.
Assim
sendo,
estudo
se
trata
revisão
sistemática
foi
construída
através
levantamento
artigos
publicados
no
período
março
2020
dezembro
2023,
tuberculose,
nas
bases
dados
SCIELO,
BVS
Pubmed.
Foram
utilizados
descritores
Vírus
SARS-CoV-2,
Mycobacterium
tuberculosis
coinfecção,
sendo
encontrados
79
excluídos
45.
No
geral,
observou-se
sintomas
mais
presentes
na
SARS-CoV-2
M.
foram
febre,
dispneia
tosse,
ambos
patógenos
podendo
invadir
qualquer
dos
sistemas
hospedeiro,
justifica
ampla
variedade
quadros
desfechos.
Com
relação
aos
biológicos,
causa
estado
inflamatório
sistêmico
desregulação
imune
caracteriza
principalmente
tempestade
citocinas
depleção
células
patógenos,
em
conjunto
torna
letal.
Frontiers in Tuberculosis,
Journal Year:
2024,
Volume and Issue:
2
Published: April 23, 2024
The
COVID
pandemic
and
tuberculosis
(TB)
endemicity
is
double
trouble
to
much
of
the
world.
SARS-CoV-2
Mycobacterium
(Mtb),
causative
agents
TB,
respectively,
are
both
infectious
respiratory
pathogens
involving
close
communities
individuals.
Both
can
cause
lung
disease,
unbalanced
inflammatory
cell
immune
responses
that
lead
a
syndemic
impact.
Moreover,
dual
infection
common
in
certain
settings.
In
low-
middle-
income
countries,
most
individuals
with
or
COVID-19,
fact,
will
have
been
exposed
infected
Mtb
some
develop
active
TB.
Here
we
review
literature
examining
diverse
interactions
M.
BCG
vaccination
SARS-CoV-2.
We
discuss
areas
which
contradictory
results
published
conclude
there
still
several
unresolved
issues
warrant
further
study
on
co-pathogenesis
BCG-
mediated
heterologous
protection
against
COVID-19.