COVID-KOSHA
Home
Help
(current)
!
Note: Language translations may be imperfect
A model anti-pandemic portal for scientists & public
Immune response
Last updated: 2022 Jan 22
Total hit(s): 7
---Sort by---
Key findings ▲
Key findings ▼
Date of publishing ▲
Date of publishing ▼
Citation Count ▲
Citation Count ▼
Impact Factor ▲
Impact Factor ▼
Select item(s)
Key Findings
Comments
(You can add your comments too!)
Original Article
(hover to see details)
Serum
samples from 28 COVID-19 convalescent patients infected with SARS-CoV-2 original strain,
Alpha,
Beta,
Gamma,
Delta,
Lambda,
and Mu variants showed 8.5, 1.2, 2.8, 1.6, 1.6, 1.7, and 4.5 folds, respectively, decreased neutralization of pseudotype SARS-CoV-2 variant
Omicron
(PV Omicron).
Despite the fact that a third-dose enhancement method can greatly raise immunity, protection from Omicron may be reduced. Hence the effectiveness of therapeutic monoclonal antibodies against the Omicron variant must be re-evaluated.
✍
34890524
(
Emerg Microbes Infect
)
PMID
34890524
Date of Publishing
: 2022 Dec
Title
The significant immune escape of pseudotyped SARS-CoV-2 variant Omicron
Author(s) name
Zhang L, Li Q et al.
Journal
Emerg Microbes Infect
Impact factor
5.84
Citation count
: 61
Date of Entry
2022 Jan 22
×
NLM format
Zhang L, Li Q, Liang Z, Li T, Liu S, Cui Q, Nie J, Wu Q, Qu X, Huang W, Wang Y. The significant immune escape of pseudotyped SARS-CoV-2 variant Omicron. Emerg Microbes Infect. 2022 Dec;11(1):1-5. PMID:34890524
The goal of this investigation was to see if
CD8+
+ T-cell responses from COVID-19 convalescent people help detect SARS-CoV-2 variants. Out of 45 mutations tested, only one in the
Beta-
variant spike matched with a previously identified low-prevalence
CD8+
+
epitope.
This means that nearly all anti-SARS-CoV-2
CD8+
+ T-cell responses should be able to recognise the newly identified variations.
✍
33594378
(
medRxiv
)
PMID
33594378
Date of Publishing
: 2021 Feb 12
Title
CD8+ T cell responses in COVID-19 convalescent individuals target conserved epitopes from multiple prominent SARS-CoV-2 circulating variants
Author(s) name
Redd AD, Nardin A et al.
Journal
medRxiv
Impact factor
- n/a -
Citation count
: 1
Date of Entry
2021 Sep 13
×
NLM format
Redd AD, Nardin A, Kared H, Bloch EM, Pekosz A, Laeyendecker O, Abel B, Fehlings M, Quinn TC, Tobian AA. CD8+ T cell responses in COVID-19 convalescent individuals target conserved epitopes from multiple prominent SARS-CoV-2 circulating variants. medRxiv. 2021 Feb 12:2021.02.11.21251585. PMID:33594378
The
serum
from 18
seropositive
healthcare workers with mild or severe SARS-CoV-2 infection were assessed for neutralization potency against the 7 potential escape mutations on
spike protein.
All samples except one showed good neutralising potency to the spike mutations and were found to be less impacted over the spike mutations against the individual mAbs.
The samples were representatives with intermediate (1:50-100), strong (1:100-1000) and potent (>1:1000) neutralizing ID50 values. The median serum ID50 for hospitalized patients selected was 1:1275, and that for selected mild/asymptomatic cases was 1:1045.
✍
33713594
(
Cell Rep
)
PMID
33713594
Date of Publishing
: 2021 Mar 23
Title
The effect of spike mutations on SARS-CoV-2 neutralization
Author(s) name
Rees-Spear C, Muir L et al.
Journal
Cell Rep
Impact factor
7.7
Citation count
: 97
Date of Entry
2021 Aug 6
×
NLM format
Rees-Spear C, Muir L, Griffith SA, Heaney J, Aldon Y, Snitselaar JL, Thomas P, Graham C, Seow J, Lee N, Rosa A, Roustan C, Houlihan CF, Sanders RW, Gupta RK, Cherepanov P, Stauss HJ, Nastouli E; SAFER Investigators, Doores KJ, van Gils MJ, McCoy LE. The effect of spike mutations on SARS-CoV-2 neutralization. Cell Rep. 2021 Mar 23;34(12):108890. PMID:33713594
The
Alpha
variant
B.1.1.7
pseudotype was evaluated for neutralization sensitivity to
serum
samples obtained from mild/asymptomatic healthcare workers and severely SARS-CoV2 affected hospitalized cohorts. The fold decrease in potency was greater for the hospitalized samples than the mild illness cohorts.
✍
33713594
(
Cell Rep
)
PMID
33713594
Date of Publishing
: 2021 Mar 23
Title
The effect of spike mutations on SARS-CoV-2 neutralization
Author(s) name
Rees-Spear C, Muir L et al.
Journal
Cell Rep
Impact factor
7.7
Citation count
: 97
Date of Entry
2021 Aug 6
×
NLM format
Rees-Spear C, Muir L, Griffith SA, Heaney J, Aldon Y, Snitselaar JL, Thomas P, Graham C, Seow J, Lee N, Rosa A, Roustan C, Houlihan CF, Sanders RW, Gupta RK, Cherepanov P, Stauss HJ, Nastouli E; SAFER Investigators, Doores KJ, van Gils MJ, McCoy LE. The effect of spike mutations on SARS-CoV-2 neutralization. Cell Rep. 2021 Mar 23;34(12):108890. PMID:33713594
The
L452R
and Y453F mutants were able to evade the cell-mediated HLA-A*24:02-restricted Cytotoxic T
lymphocytes
(CTL) responses as well as acquired immunity(humoral immunity) of the host during infection
These mutants were able to escape both natural and acquired immune systems and also had a higher virulence factor proving their lethality. The increased binding affinity of the ACE2 receptor eventually increased the virulence and viral replication factors. L452R mutation increased protein stability, viral infectivity, and potentially promotes viral replication. L452R mutant also showed increased infectivity in pseudoviruses.
✍
doi
Title
An emerging SARS-CoV-2 mutant evading cellular immunity and increasing viral infectivity
Impact factor
N/A
Date of Entry
2021 Aug 6
The T-cell responses to the wild-type
spike protein
were more robust in vaccinated individuals when compared to convalescent patients.
✍
Pre-print
(
bioRXiv
)
Date of Publishing
2021 May 03
Title
SARS -CoV-2 T-cell immunity to variants of concern following vaccination
Impact factor
N/A
Date of Entry
2021 Jul 2
Decreased T-cell responses were observed in response to the
spike protein
from 3 variants of the virus
-B.1.1.7,
B.1.351,
and B.1.1.248 (when compared to wildtype spike) in vaccinated individuals
✍
Pre-print
(
bioRXiv
)
Date of Publishing
2021 May 03
Title
SARS -CoV-2 T-cell immunity to variants of concern following vaccination
Impact factor
N/A
Date of Entry
2021 Jul 2