An Individual’s First Encounter With The Type Of Flu Virus Is Extremely Important
Source: Thailand Medical News Jan 06, 2020 4 years, 11 months, 2 weeks, 5 days, 18 hours, 8 minutes ago
A new study shows that
the first strain of
influenza virus we encounter during childhood sets the course of how our immune system responds to exposures later in life.
How successfully a person can fend off the
flu depends not only on the virus’ notorious ability to change with the season, but also on the strain first encountered during childhood, according to new research published in the open-access journal
PLoS Pathogens.
The study findings offer an explanation for why some patients fare much worse than others when infected with the same strain of the
flu virus. The results also could help inform strategies aimed at curbing the impact from the seasonal
flu.
Study co-author Dr Michael Worobey, head of the Department of Ecology and Evolutionary Biology and a member of the BIO5 Institute at the University of Arizona told
Thailand Medical New, “The last two
flu seasons have been more severe than expected. In the 2017-18 season, 80,000 people died in the U.S., more than in the swine
flu pandemic of 2009.
Influenza is a major, major killer not just in this country, but worldwide.”
For years, scientists and healthcare professionals were vexed by the fact that the same strain of the
flu virus affects people to various degrees of severity. Then, in 2016, a team including Worobey and authors of the current study presented a paper in the journal Science showing that past exposure to the
flu virus determines an individual’s response to subsequent infections, a phenomenon called immunological imprinting.
The new discovery helped overturn the prior commonly held belief that previous exposure to a
flu virus conferred little or no immunological protection against strains that can jump from animals into humans, such as those causing the so-called swine
flu or bird
flu. These strains, which have already caused hundreds of spillover cases of severe illness or death in humans, are of global concern because they could gain mutations that allow them not only to readily jump from animal populations to humans, but also spread rapidly from person to person.
The researchers in the current study, set out to investigate whether immunological imprinting could explain people’s response to
flu strains already circulating in the human population and to what extent it could account for observed discrepancies in how severely the seasonal
flu affects different age groups.
The research team analyzed health records that the Arizona Department of Health Services routinely obtains from hospitals and private physicians to track
flu cases to study how different strains of the flu virus affect people at different ages.
Typically, two subtypes of
influenza virus,
H3N2 and
H1N1, have been respons
ible for seasonal outbreaks of the
flu over the last several decades.
H3N2 causes the majority of severe, clinically attended cases in high-risk elderly cohorts and the majority of overall deaths.
H1N1 causes fewer deaths overall and skews more toward young and middle-aged adults.
The meta analysis of the health record data revealed a pattern: People first exposed to
H1N1 during childhood were less likely to end up hospitalized if they encountered
H1N1 again later in life than people who were first exposed to
H3N2. Conversely, those first exposed to
H3N2 enjoyed extra protection against
H3N2 later in life.
To properly understand the discrepancy, the researchers dug into the evolutionary relationships between
influenza virus strains.
H1N1 and
H3N2, it turned out, belong to two separate branches, or groups, on the
influenza “family tree.” While infection with one does result in the immune system being better prepared to fight a future infection from the other, the protection against future infections is much stronger when exposed to strains from the same group it has battled before.
Dr Worobey added, “In other words, if you were a child and had your first bout of flu in 1955, when the
H1N1 but not
H3N2 virus was circulating, an infection with
H3N2 was much more likely to land you in the hospital than an infection with
H1N1 last year, when both strains were circulating.”
The records also revealed another pattern, one that was much more difficult to explain: People whose first childhood exposure was to
H2N2, a close cousin of
H1N1, did not have a protective advantage when they later encountered
H1N1. This seemed strange, as the two subtypes are in the same group, and the researchers’ earlier work showed that exposure to one can, in some cases, grant considerable protection against the other.
Lead author Dr Katelyn Gostic, who conducted this research as a doctoral student in the lab of the paper’s senior author, Dr James Lloyd-Smith, at the University of California, Los Angeles commented, “Our immune system often struggles to recognize and defend against closely related strains of seasonal
flu, even though these are essentially the genetic sisters and brothers of strains that circulated just a few years ago. This is perplexing because our research on bird
flu shows that deep in our immune memory, we have some ability to recognize and defend against the distantly related, genetic third cousins of the strains we saw as children.”
Dr Worobey further added, “Clearly, something compromises the immunity to strains that you see secondarily, even if they belong to the same group as your first exposure. The second subtype you’re exposed to is not able to create an immune response that is as protective and durable as the first.”
Basically, our ability to fight off the
flu virus is determined not only by the subtypes we have encountered over the course of our lives, but also by the sequence in which we have encountered them.
Dr Worobey says, “Whichever subtype our immune system sees first lays down an imprint that protects us especially well against strains of the same subtype, but relatively poorly against strains from other subtypes, even though you’ve encountered those subsequently.”
The detailed molecular causes of this effect are currently being studied, according to the researchers.
Dr Worobey further added, “Part of your immune system’s response to current infection is directed against the strain you first had as a kid, and that investment of fighting the last war appears to compromise your ability to form a fully effective immune response to the invader you encounter later.”
The medical researchers hope that their findings may help predict which age groups might be severely affected during future
flu seasons based on the subtype circulating, which in turn may help health officials prepare an adequate response, such as doling out limited vaccines by cohort.
Dr Shane Brady, Deputy State Epidemiologist at the Arizona Department of Health Services in Phoenix commented, “These findings provide insight into the patterns we see in our
flu surveillance and how they might change in the future. This highlights the importance of collaboration between public health practitioners and researchers.”
The research study adds to earlier work by the same group that has made the concept of immunological imprinting a key part of the long-term battle against
flu and one of the foundations of the National Institutes of Health’s strategic plan to develop a universal
flu vaccine.
Dr Gostic added, “We hope that by studying differences in immunity against bird
flus, where our immune system shows a natural ability to deploy broadly effective protection, and against seasonal
flus, where our immune system seems to have bigger blind spots, we can uncover clues useful to universal
influenza vaccine development.”
Dr Worobey concluded, “We need a vaccine that targets the deficits on an individualized level. Our work has clearly shown that the first virus we had can have a profound long-term effect. The bad side of that is that our immune system seems to be locked into fighting just one half of
flu genetic diversity, and we need to find ways of breaking that.”
Reference: “Childhood immune imprinting to influenza A shapes birth year-specific risk during seasonal H1N1 and H3N2 epidemics” by Katelyn M. Gostic ,Rebecca Bridge, Shane Brady, Cécile Viboud, Michael Worobey and James O. Lloyd-Smith, 19 December 2019, PLoS Pathogens.DOI: 10.1371/journal.ppat.1008109