Researchers at Boston Children's Hospital reports that a common fungal infection can trigger asthma and make it much worse by way of a route not targeted by existing asthma drugs. Their findings were published on Nature Medicine which had implications for some patients with severe asthma who may be chronically exposed to fungi and can become highly sensitized.
The findings from this mouse study explain why existing asthma drugs don't work well in fungal-associated asthma. "As we understand the different pathways to asthma, we can develop better therapies," says senior investigator Dale Umetsu, MD, PhD, of Boston Children's Division of Immunology and also a professor at Harvard Medical School. "Most existing therapies are good for allergic asthma, but they're not effective in many patients, whose asthma may involve non-classical pathways."
When Umetsu and colleagues exposed the mice to the fungus Aspergillus fumigatus, a mold common in the indoor and outdoor environment, they developed airway hyperreactivity, the cardinal feature of asthma, within just a few days. Since allergic responses in mice typically take 10 to 14 days to develop, this finding suggested that the fungus triggers an immediate, innate immune response.
Traditional asthma-control drugs, such as inhaled corticosteroids, act on pathways involving Th2 cells, a type of T cell in the adaptive immune system that is important in allergy. However, the new study shows, in mice and in human cell cultures, that Aspergillus directly activates a recently discovered group of T cells, known as natural killer T cells (NKT cells), via a lipid molecule on its surface, asperamide B. In live mice, asperamide B alone was enough to induce airway hyperreactivity.
Umetsu and colleagues first showed in 2006 that NKT cells can trigger asthma in people in the absence of Th2 cells. The cells have been shown to be activated by various bacteria, but this is the first demonstration of their activation by a fungus.
Although Aspergillus and NKT cells initiate asthma through non-allergic means, patients can become sensitized to the fungus and develop chronic allergic reactions that make their respiratory disease more severe. Previous studies indicate that 28 per cent of patients with asthma and 45 per cent of patients with severe asthma become sensitized to Aspergillus.
Umetsu's investigations support the growing idea that asthma is a collection of different disease processes that all cause airways to become twitchy and constricted. In 2011, for example, his lab showed that influenza infection—which often requires asthmatic children to be hospitalized—exacerbates asthma by activating not Th2 cells or NKT cells, but yet another group of immune cells called natural helper cells or innate lymphoid cells.
"We need to understand the specific asthma pathways present in each individual with asthma and when they are triggered, so we can give the right treatment at the right time," Umetsu says.
Some academic research groups are using antifungal agents in asthma, with some success, Umetsu notes. In the future, he would like to target NKT cells in patients with severe asthma if a successful targeting method could be found.
The paper's first author was Lee Albacker, PhD, of the Division of Immunology at Boston Children's Hospital, who worked on the study as a graduate student in the Immunology Programme at Harvard University. Coauthors were Vinod Chaudhary, PhD, and Paul Savage, PhD, of Brigham Young University, and Ya-Jen Chang, PhD, Hye Young Kim, PhD, Ya-Ting Chuang, PhD, Muriel Pichavant, PhD, Rosemarie DeKruyff, PhD, of Boston Children's Hospital.
The study was supported by the National Institute of Allergy and Infectious Diseases, the National Heart Lung Blood Institute (grants RO1AI026322, RC1HL099839 and R21AI083523) and by the Bunning Food Allergy Project.
Boston Children's Hospital is home to the world's largest research enterprise based at a pediatric medical center, where its discoveries have benefited both children and adults. Founded as a 20-bed hospital for children, Boston Children's today is a 395 bed comprehensive center for pediatric and adolescent health care grounded in the values of excellence in patient care and sensitivity to the complex needs and diversity of children and families.
Source:Pharmabiz
The findings from this mouse study explain why existing asthma drugs don't work well in fungal-associated asthma. "As we understand the different pathways to asthma, we can develop better therapies," says senior investigator Dale Umetsu, MD, PhD, of Boston Children's Division of Immunology and also a professor at Harvard Medical School. "Most existing therapies are good for allergic asthma, but they're not effective in many patients, whose asthma may involve non-classical pathways."
When Umetsu and colleagues exposed the mice to the fungus Aspergillus fumigatus, a mold common in the indoor and outdoor environment, they developed airway hyperreactivity, the cardinal feature of asthma, within just a few days. Since allergic responses in mice typically take 10 to 14 days to develop, this finding suggested that the fungus triggers an immediate, innate immune response.
Traditional asthma-control drugs, such as inhaled corticosteroids, act on pathways involving Th2 cells, a type of T cell in the adaptive immune system that is important in allergy. However, the new study shows, in mice and in human cell cultures, that Aspergillus directly activates a recently discovered group of T cells, known as natural killer T cells (NKT cells), via a lipid molecule on its surface, asperamide B. In live mice, asperamide B alone was enough to induce airway hyperreactivity.
Umetsu and colleagues first showed in 2006 that NKT cells can trigger asthma in people in the absence of Th2 cells. The cells have been shown to be activated by various bacteria, but this is the first demonstration of their activation by a fungus.
Although Aspergillus and NKT cells initiate asthma through non-allergic means, patients can become sensitized to the fungus and develop chronic allergic reactions that make their respiratory disease more severe. Previous studies indicate that 28 per cent of patients with asthma and 45 per cent of patients with severe asthma become sensitized to Aspergillus.
Umetsu's investigations support the growing idea that asthma is a collection of different disease processes that all cause airways to become twitchy and constricted. In 2011, for example, his lab showed that influenza infection—which often requires asthmatic children to be hospitalized—exacerbates asthma by activating not Th2 cells or NKT cells, but yet another group of immune cells called natural helper cells or innate lymphoid cells.
"We need to understand the specific asthma pathways present in each individual with asthma and when they are triggered, so we can give the right treatment at the right time," Umetsu says.
Some academic research groups are using antifungal agents in asthma, with some success, Umetsu notes. In the future, he would like to target NKT cells in patients with severe asthma if a successful targeting method could be found.
The paper's first author was Lee Albacker, PhD, of the Division of Immunology at Boston Children's Hospital, who worked on the study as a graduate student in the Immunology Programme at Harvard University. Coauthors were Vinod Chaudhary, PhD, and Paul Savage, PhD, of Brigham Young University, and Ya-Jen Chang, PhD, Hye Young Kim, PhD, Ya-Ting Chuang, PhD, Muriel Pichavant, PhD, Rosemarie DeKruyff, PhD, of Boston Children's Hospital.
The study was supported by the National Institute of Allergy and Infectious Diseases, the National Heart Lung Blood Institute (grants RO1AI026322, RC1HL099839 and R21AI083523) and by the Bunning Food Allergy Project.
Boston Children's Hospital is home to the world's largest research enterprise based at a pediatric medical center, where its discoveries have benefited both children and adults. Founded as a 20-bed hospital for children, Boston Children's today is a 395 bed comprehensive center for pediatric and adolescent health care grounded in the values of excellence in patient care and sensitivity to the complex needs and diversity of children and families.
Source:Pharmabiz
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