Latest News !!! Current Covid Vaccine Protects Against Delta's Severe Consequences, Omicron: Study
The Beth Israel Deaconess Medical Center (BIMC) team in Israel evaluated a sample of 47 people who were vaccinated with either the Johnson & Johnson or Pfizer-BioNTech vaccine.
Jerusalem: Current COVID-19 vaccination
provides strong protection against severe illness and hospitalization caused by
the Delta and Omicron variants, according to a study.
A study published in the journal Nature on
Monday showed that vaccination induces this protection through cellular
immunity, or the production of protective immune cells such as so-called killer
cells and memory cells.
The researchers say that cellular immunity
continues to protect against severe COVID-19 disease even though the Omicron
variant evades neutralizing antibodies.
The Beth Israel Deaconess Medical Center
(BIDMC) team in Israel evaluated samples from 47 people vaccinated with either
the Johnson & Johnson or Pfizer-BioNTech vaccine.
"Our data provide an immunological context
for observing that current vaccines continue to provide strong protection
against severe illness and hospitalization due to the Omicron variant, despite
a significant reduction in neutralizing antibody response and an increase in
breakthrough infection," said related author Dan H. Barush.
The researchers used samples from uninfected
people who had received either the Johnson & Johnson or Pfizer vaccines.
They measured the response of CD8+ T cells and
CD4+ T cells to the original Delta and Omicron SARS-CoV-2 strain for one month
and then eight months after the final vaccination.
CD4 and CD8 cells, also known as T cells, are
white blood cells that fight infection and play an important role in the immune
system.
The team also assessed antibody response to variants
at one and eight months. In line with previous research, the scientists found a
minimally reactive cross-neutralizing antibody that is specific for Omicron.
In contrast, the data show that the
Omicron-specific CD8+ T-cell response is more than 80% cross-reactive compared
to the CD8+ T-cell response to the host viral strain.
Similarly, more than 80% of Omicron-specific
CD4+ T cells showed cross-reactivity, although responses may vary from person
to person, the researchers noted.
"Given the role of CD8+ T cells in
clearing viral infection, it is likely that cellular immunity makes a
significant contribution to vaccine protection against severe SARS-CoV-2
disease," said Barush, whose team was involved in the development of the
Johnson and Johnson vaccine. .
"This may be especially true for Omicron,
which drastically evades the neutralizing antibody response," he said. .
This is due to its ability to evade
virus-killing neutralizing antibodies that the body produces in response to
vaccination.
This report is
generated automatically by PTI News Service. ThePrint is not responsible for
its contents.
Overview
Cellular immunity is an immune response that does not
include antibodies, but includes the activation of phagocytes, specific
cytotoxic T lymphocytes, and the release of various cytokines in response to
antigens.
Historically, the immune system has been divided into two
branches: humoral immunity, in which the protective function of immunization
can be found in humor (biological fluid or cell-free serum), and cellular
immunity, in which the protective function of immunity lies in cell-bound. .
CD4 cells or T-helper cells provide protection against various pathogens. Naive
T cells, mature T cells that never encounter an antigen, turn into active
effector T cells when they encounter antigen presenting cells (APCs).
These APCs, like macrophages, dendritic cells, and B cells
under some circumstances, load antigenic peptides onto MHC cells, in turn
presenting the peptides to receptors on T cells. The most important of these
APCs are highly specialized dendritic cells; conceivably operate solely to
ingest and present antigen.
Activated Effector T cells can be assigned to three
functional classes, detecting peptide antigens derived from different types of
pathogens: The first class is cytotoxic T cells, which kill target cells
infected by apoptosis without the use of cytokines, the second class is TH1
cells, which mainly function to activate macrophages, and the third class is
TH2 cells, whose main function is to stimulate B cells to produce antibodies.
The
innate immune system and the adaptive immune system consist of humoral and
cell-mediated components, respectively.
Cellular immunity protects the body by:
Cells such as killer T cells, macrophages, natural killer cells among the immunological reactions that eliminate pathogens themselves, virus-infected cells, cancer cells, etc. This is referred to as humoral immunity (humoral immunity), where the subject of elimination is antibodies in body fluids. Delayed responses such as rejection reactions and contact dermatitis after organ transplantation are also cellular immunity. → lymphocyte / allergy
Pfizer Covid-19 Vaccine
On July 14, 2021, the POM has issued the EUA for one type
of Covid-19 vaccine developed on the mRNA platform, namely the Comirnaty
Vaccine produced by Pfizer and BioNTech. Based on phase 3 clinical trial data,
the efficacy of Pfizer's Covid-19 vaccine at the age of 16 years and over
showed 95.5% success.
Meanwhile, the efficacy of Pfizer's Covid-19 vaccine in
adolescents aged 12-15 years is 100 percent. Immunogenicity data also showed
that administration of 2 doses of Comirnaty vaccine at 3 weeks interval resulted
in a good immune response. As vaccines with mRNA platforms that have special
storage specifications using ultra low temperatures, namely at -90 to -60
degrees Celsius.
The reactions or side effects that most often arise from
the use of the Pfizer vaccine include pain at the injection site, fatigue,
headache, muscle aches, chills, joint pain, and fever.
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