1.Detection of serum immunoglobulin M and immunoglobulin G antibodies in 2019 novel coronavirus infected patients from different stages.
Hui-Xia GAO ; Ya-Nan LI ; Zun-Gui XU ; Yu-Ling WANG ; Hai-Bin WANG ; Jin-Feng CAO ; De-Qin YUAN ; Li LI ; Yi XU ; Zhi ZHANG ; Ying HUANG ; Jian-Hua LU ; Yu-Zhen LIU ; Er-Hei DAI
Chinese Medical Journal 2020;133(12):1479-1480
2.Strategies for vaccine development of COVID-19.
Limin YANG ; Deyu TIAN ; Wenjun LIU
Chinese Journal of Biotechnology 2020;36(4):593-604
An epidemic of acute respiratory syndrome in humans, which appeared in Wuhan, China in December 2019, was caused by a novel coronavirus (SARS-CoV-2). This disease was named as "Coronavirus Disease 2019" (COVID-19). SARS-CoV-2 was first identified as an etiological pathogen of COVID-19, belonging to the species of severe acute respiratory syndrome-related coronaviruses (SARSr-CoV). The speed of both the geographical transmission and the sudden increase in numbers of cases is much faster than SARS and Middle East respiratory syndrome (MERS). COVID-19 is the first global pandemic caused by a coronavirus, which outbreaks in 211 countries/territories/areas. The vaccine against COVID-19, regarded as an effective prophylactic strategy for control and prevention, is being developed in about 90 institutions worldwide. The experiences and lessons encountered in the previous SARS and MERS vaccine research can be used for reference in the development of COVID-19 vaccine. The present paper hopes to provide some insights for COVID-19 vaccines researchers.
Betacoronavirus
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immunology
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Biomedical Research
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Coronavirus Infections
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epidemiology
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immunology
;
prevention & control
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virology
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Humans
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Internationality
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Middle East Respiratory Syndrome Coronavirus
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immunology
;
Pandemics
;
prevention & control
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Pneumonia, Viral
;
epidemiology
;
immunology
;
prevention & control
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virology
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SARS Virus
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immunology
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Severe Acute Respiratory Syndrome
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immunology
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Viral Vaccines
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immunology
3.Coagulation and immune function indicators for monitoring of coronavirus disease 2019 and the clinical significance.
Junhua ZHANG ; Tie LI ; Rong HUANG ; Rong GUI ; Sai CHEN
Journal of Central South University(Medical Sciences) 2020;45(5):525-529
OBJECTIVES:
To explore the significance of coagulation and immune function indicators in clinical diagnosis and treatment of coronavirus disease 2019 (COVID-19).
METHODS:
All patients with COVID-19 diagnosed and treated in First People's Hospital of Yueyang from January to March 2020 were enrolled. The general data of patients were collected. The patients were assigned into a light group (=20), an ordinary group (=33), a severe group (=23), and a critically severe group (=7) according to the severity of the disease. Coagulation and immune function indicators of each group were compared, and the relevance of coagulation and immune function indicators was analyzed.
RESULTS:
The age of COVID-19 patients in Yueyang City was mainly between 45 and 65 years old. There was a significant difference in the coagulation function and immune-related indicators in each group of patients (all <0.05).
CONCLUSIONS
There are some abnormalities in coagulation and immune function in patients with COVID-19, which possess significance for clinical diagnosis and treatment of the disease.
Aged
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Betacoronavirus
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Blood Coagulation
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China
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Coronavirus Infections
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diagnosis
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immunology
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Humans
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Immune System
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physiopathology
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Middle Aged
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Pandemics
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Pneumonia, Viral
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diagnosis
;
immunology
4.Immunomodulatory therapy of cytomegalovirus pneumonia after liver transplantation.
Gen-shu WANG ; Gui-hua CHEN ; Min-qiang LU ; Yang YANG ; Chang-jie CAI ; Hui-min YI ; Hua LI ; Chi XU ; Shu-hong YI
Chinese Medical Journal 2006;119(17):1430-1434
BACKGROUNDThere has been increasing interest in the research into cytomegalovirus (CMV) pneumonia after liver transplantation (LT). This study was undertaken to investigate the immunomodulatory therapy of CMV pneumonia after LT.
METHODSSix patients with CMV pneumonia after LT from October 2003 to November 2005 were analyzed retrospectively. They were diagnosed according to clinical manifestations, chest X-ray findings and pathogenic changes and given comprehensive therapy including mainly immunomodulation therapy and anti-viral medication. At the early stage of CMV pneumonia, the dose of immunosuppressive agents was decreased or ceased, instead replaced by immunoenhancement therapy. During recovery period from CMV pneumonia, the dose of immunosuppressive agents was given again or enhanced, and immunoenhancement therapy was ceased. The liver function of the patients was monitored closely during the treatment.
RESULTSIn this series, five patients were survived and one died. The liver function of the six patients remained normal during the treatment, and no episode of acute rejection took place.
CONCLUSIONSPoor immunity is the pathogenic basis of CMV pneumonia after LT. At early stage of CMV pneumonia, the immunity of the patients should be enhanced, and during the recovery period from CMV pneumonia, immunosuppressants should be given again but immunoenhancement therapy ceased. Individualized immunomodulatory therapy is essential to the treatment of CMV pneumonia after LT.
Adjuvants, Immunologic ; therapeutic use ; Adult ; Cytomegalovirus Infections ; drug therapy ; immunology ; Humans ; Liver Transplantation ; adverse effects ; immunology ; Lymphocyte Activation ; Male ; Middle Aged ; Pneumonia, Viral ; drug therapy ; immunology
5.Cytomegalovirus Pneumonia: High - Resolution CT Findings in Ten Non-AIDS Immunocompromised Patients.
Jeung Hee MOON ; Eun A KIM ; Kyung Soo LEE ; Tae Sung KIM ; Kyung Jae JUNG ; Jae Hoon SONG
Korean Journal of Radiology 2000;1(2):73-78
OBJECTIVE: To describe the HRCT findings of cytomegalovirus (CMV) pneumonia in non-AIDS immunocompromised patients. MATERIALS AND METHODS: This retrospective study involved the ten all non-AIDS immunocompromised patients with biopsy-proven CMV pneumonia and without other pulmonary infection encountered at our Medical Center between January 1997 and May 1999. HRCT scans were retrospectively analysed by two chest radiologists and decisions regarding the findings were reached by consensus. RESULTS: The most frequent CT pattern was ground-glass opacity, seen in all patients, with bilateral patchy (n = 8) and diffuse (n = 2) distribution. Other findings included poorly-defined small nodules (n = 9) and consolidation (n = 7). There was no zonal predominance. The small nodules, bilateral in eight cases and unilateral in one, were all located in the centrilobular region. Consolidation (n = 7), with patchy distribution, was bilateral in five of seven patients (71%). Pleural effusion and bilateral areas of thickened interlobular septa were seen in six patients (60%). CONCLUSION: CMV pneumonia in non-AIDS immunocompromised patients appears on HRCT scans as bilateral mixed areas of ground-glass opacity, poorly-defined centrilobular small nodules, and consolidation. Interlobular septal thickening and pleural effusion are frequently associated.
Cytomegalovirus Infections/immunology/*radiography
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Female
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Human
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Immunocompromised Host/*immunology
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Male
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Middle Age
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Pneumonia, Viral/immunology/*radiography/virology
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Retrospective Studies
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Tomography, X-Ray Computed/*methods
6.Cytomegalovirus Pneumonia: High - Resolution CT Findings in Ten Non-AIDS Immunocompromised Patients.
Jeung Hee MOON ; Eun A KIM ; Kyung Soo LEE ; Tae Sung KIM ; Kyung Jae JUNG ; Jae Hoon SONG
Korean Journal of Radiology 2000;1(2):73-78
OBJECTIVE: To describe the HRCT findings of cytomegalovirus (CMV) pneumonia in non-AIDS immunocompromised patients. MATERIALS AND METHODS: This retrospective study involved the ten all non-AIDS immunocompromised patients with biopsy-proven CMV pneumonia and without other pulmonary infection encountered at our Medical Center between January 1997 and May 1999. HRCT scans were retrospectively analysed by two chest radiologists and decisions regarding the findings were reached by consensus. RESULTS: The most frequent CT pattern was ground-glass opacity, seen in all patients, with bilateral patchy (n = 8) and diffuse (n = 2) distribution. Other findings included poorly-defined small nodules (n = 9) and consolidation (n = 7). There was no zonal predominance. The small nodules, bilateral in eight cases and unilateral in one, were all located in the centrilobular region. Consolidation (n = 7), with patchy distribution, was bilateral in five of seven patients (71%). Pleural effusion and bilateral areas of thickened interlobular septa were seen in six patients (60%). CONCLUSION: CMV pneumonia in non-AIDS immunocompromised patients appears on HRCT scans as bilateral mixed areas of ground-glass opacity, poorly-defined centrilobular small nodules, and consolidation. Interlobular septal thickening and pleural effusion are frequently associated.
Cytomegalovirus Infections/immunology/*radiography
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Female
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Human
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Immunocompromised Host/*immunology
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Male
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Middle Age
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Pneumonia, Viral/immunology/*radiography/virology
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Retrospective Studies
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Tomography, X-Ray Computed/*methods
7.Coronavirus Disease 2019 Influenza A in Children: An Observational Control Study in China.
Yang ZHAO ; De Lin SUN ; Heather C BOUCHARD ; Xin Xin ZHANG ; Gang WAN ; Yi Wei HAO ; Shu Xin HE ; Yu Yong JIANG ; Lin PANG
Biomedical and Environmental Sciences 2020;33(8):614-619
This study aimed to understand the differences in clinical, epidemiological, and laboratory features between the new coronavirus disease 2019 (COVID-2019) and influenza A in children. Data of 23 hospitalized children with COVID-19 (9 boys, 5.7 ± 3.8 years old) were compared with age- and sex-matched 69 hospitalized and 69 outpatient children with influenza A from a hospital in China. The participants' epidemiological history, family cluster, clinical manifestations, and blood test results were assessed. Compared with either inpatients or outpatients with influenza A, children with COVID-19 showed significantly more frequent family infections and higher ratio of low fever (< 37.3 °C), but shorter cough and fever duration, lower body temperature, and lower rates of cough, fever, high fever (> 39 °C), nasal congestion, rhinorrhea, sore throat, vomiting, myalgia or arthralgia, and febrile seizures. They also showed higher counts of lymphocytes, T lymphocyte CD8, and platelets and levels of cholinesterase, aspartate aminotransferase, lactate dehydrogenase, and lactic acid, but lower serum amyloid, C-reactive protein, and fibrinogen levels and erythrocyte sedimentation rate, and shorter prothrombin time. The level of alanine aminotransferase in children with COVID-19 is lower than that in inpatients but higher than that in outpatients with influenza A. Pediatric COVID-19 is associated with more frequent family infection, milder symptoms, and milder immune responses relative to pediatric influenza A.
Betacoronavirus
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physiology
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Case-Control Studies
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Child
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Coronavirus Infections
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blood
;
epidemiology
;
immunology
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virology
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Female
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Humans
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Influenza, Human
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blood
;
epidemiology
;
immunology
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Male
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Pandemics
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Pneumonia, Viral
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blood
;
epidemiology
;
immunology
;
virology
8.From H1N1 to 2019-nCoV, what do we learn?
Gui-E LIU ; Yuan TIAN ; Wen-Jun ZHAO ; Shuang-Ming SONG ; Lei LI
Chinese Journal of Traumatology 2020;23(4):187-189
The COVID-19 pandemic is still raging across the world. Everyday thousands of infected people lost their lives. What is worse, there is no specific medicine and we do not know when the end of the pandemic will come. The nearest global pandemic is the 1918 influenza, which caused about 50 million deaths and partly terminate the World War Ⅰ. We believe that no matter the virus H1N1 for the 1918 influenza or 2019-nCoV for COVID-19, they are essentially the same and the final cause of death is sepsis. The definition and diagnostic/management criteria of sepsis have been modified several times but the mortality rate has not been improved until date. Over decades, researchers focus either on the immunosuppression or on the excessive inflammatory response following trauma or body exposure to harmful stimuli. But the immune response is very complex with various regulating factors involved in, such as neurotransmitter, endocrine hormone, etc. Sepsis is not a kind of disease, instead a misbalance of the body following infection, trauma or other harmful stimulation. Therefore we should re-think sepsis comprehensively with the concept of systemic biology, i.e. inflammationomics.
Betacoronavirus
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Coronavirus Infections
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complications
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epidemiology
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immunology
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Humans
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Immune Tolerance
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Inflammation
;
complications
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Influenza A Virus, H1N1 Subtype
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Influenza, Human
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complications
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epidemiology
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immunology
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Pandemics
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Pneumonia, Viral
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complications
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epidemiology
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immunology
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Sepsis
;
etiology
9.A rapid colloidal gold immunochromatographic assay for the diagnosis of coronavirus disease 2019.
Xiao-Ling WANG ; Lei WANG ; Chao-Lu HASI ; Yu-Po WANG ; Ajab KHAN ; Bin-Zhi REN ; Zhi-Zhen LIU ; Shun-Lin HOU ; Li-Hong YANG ; Liao-Yun ZHANG ; Yong-Kang DONG ; Jun XU ; Jun XIE
Chinese Medical Journal 2020;133(16):1986-1988
10.Monitoring of influenza virus B and clinical features of pediatric pneumonia caused by influenza virus B only.
Jun HUA ; Xiao-Chen DU ; Min-Hui XIE ; Xue-Lan ZHANG ; Yun-Fang DING ; Wei JI
Chinese Journal of Contemporary Pediatrics 2012;14(11):830-833
OBJECTIVETo investigate the epidemiological features of influenza virus B (IVB) in the winter and the clinical features of pediatric pneumonia caused by IVB only.
METHODSA retrospective study was performed on the clinical data of children with respiratory infection who received pathogen testing and therapy at Soochow University Affiliated Children's Hospital during the winters of 2008, 2009, 2010 and 2011.
RESULTSThe positive rates of influenza viruses A and B in the winters of 2008, 2009, and 2010 were 0.89%, 5.49%, and 6.24% respectively; the positive rate of influenza viruses A and B in the winter of 2011 was 8.72%, significantly higher than those in 2008-2010. The positive rates of IVB in the winters of 2008, 2009, and 2010 were 0%, 0%, and 0.21% respectively; the positive rate of IVB in the winter of 2011 was 5.36%, which was significantly higher than in the years 2008 to 2010. Pneumonia caused by IVB was confirmed in 94 children during the winter of 2011, including 27 cases of pneumonia caused by IVB only. Most of children with pneumonia caused by IVB only were aged over 6 months. The common symptoms in the 27 children caused by IVB only were fever (85%), runny nose (89%), and cough (100%). Wheezing (26%) and dyspnea (7%) were also seen in some cases. Among the 27 children, 19% showed abnormal white blood cell count, 30% showed increased C-reactive protein, 70% showed decreased prealbumin, and none showed visible organ dysfunction. No specific imaging findings were seen in the children with pneumonia caused by IVB only. However, many abnormal humoral and cellular immunological parameters were found in the majority of these children. The average length of hospital stay was approximately one week, there were no critical patients and the prognosis was good.
CONCLUSIONSInfluenza viruses were at a peak level in inpatient children in the winter of 2011. IVB infection rate was gradually increasing. In children with pneumonia caused by IVB only, there are few critical patients, the symptoms are nonspecific and the prognosis is good.
Adolescent ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Infant, Newborn ; Influenza B virus ; Influenza, Human ; diagnosis ; epidemiology ; immunology ; Length of Stay ; Male ; Pneumonia, Viral ; diagnosis ; epidemiology ; immunology ; Retrospective Studies