Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 15, Number 3—March 2009

Meeting the Challenge of Influenza Pandemic Preparedness in Developing Countries

David S. FedsonComments to Author 
Author affiliation: University of Virginia, Charlottesville, Virginia, USA (retired)

Cite This Article


Developing countries face unique difficulties preparing for an influenza pandemic. Our current top-down approach will not provide these countries with adequate supplies of vaccines and antiviral agents. Consequently, they will have to use a bottom-up approach based on inexpensive generic agents that either modify the host response to influenza virus or act as antiviral agents. Several of these agents have shown promise, and many are currently produced in developing countries. Investigators must primarily identify agents for managing infection in populations and not simply seek explanations for how they work. They must determine in which countries these agents are produced and define patterns of distribution and costs. Because prepandemic research cannot establish whether these agents will be effective in a pandemic, randomized controlled trials must begin immediately after a new pandemic virus has emerged. Without this research, industrialized and developing countries could face an unprecedented health crisis.

More than a decade ago, the first human cases of disease caused by avian influenza virus A (H5N1) appeared in Hong Kong Special Administrative Region, People’s Republic of China. Five years ago, influenza virus A (H5N1) reemerged to cause highly lethal human disease in Southeast Asia. Health officials are concerned that these cases could be the harbinger of the next influenza pandemic. As a result, virtually all industrialized countries and many developing countries have mounted extensive pandemic preparedness efforts. However, as pointed out recently by Oshitani et al., industrialized countries face “unique and difficult issues, which make preparing for a pandemic more challenging” (1).

Why a Top-Down Approach to Confronting the Next Pandemic Will Not Work

If a pandemic form of influenza virus A (H5N1) emerges within the next few years, all countries will have to depend almost entirely on egg-derived inactivated adjuvanted influenza vaccines. For developing countries, this approach will not succeed. Estimates show that within the first 6–9 months of a pandemic outbreak, vaccine companies will be only able to produce enough doses to vaccinate ≈700 million persons (2). This number is less than the combined populations of the 9 countries that produce almost all of the world’s seasonal influenza vaccines. These countries will first use their vaccines to ensure that their own populations are protected. Non–vaccine-producing countries, both industrialized and developing, will have to wait.

In 2005, a representative of the World Health Organization (WHO) Global Programme on Influenza concluded that “most developing countries will have no access to a vaccine during the first wave of a pandemic and perhaps throughout its duration” (2). Since then, WHO has worked to build a stockpile of ≈1500 million doses of vaccine against influenza virus A (H5N1) for developing countries (3), and 2 companies have pledged to provide WHO with 110 million doses. In 2007, a WHO scientific consultation on how to use this stockpile concluded, “If there is sufficient early warning that an outbreak of influenza (H5N1) is due to a virus that is capable of sustained human-to-human transmission, then theoretically there may be a relatively limited ‘window of opportunity’ to stop the spread of the virus before it spreads nationally or internationally. … However, a containment effort would be feasible only in settings where the number of localized cases are [sic] still limited, where adequate logistical support is available, and where the national government is supported by international assistance” (3). The vaccine stockpile on which these efforts would depend does not yet exist.

Several industrialized countries are stockpiling vaccines against influenza virus A (H5N1) that might be used for prepandemic vaccination, but Oshitani et al. note that “both pandemic and prepandemic vaccines would not be available in developing countries unless an international mechanism exists to share such vaccine with them at low cost” (1). Even if limited supplies of vaccines could be produced for developing countries, no international mechanism is in place to pay for and distribute the vaccines, and WHO has yet to announce plans to set one up. Thus, when the next pandemic virus emerges, almost no vaccines will be available in developing countries to slow its spread (1,2).

Because global supplies of vaccines against pandemic viruses will be limited, government officials in a few industrialized countries have placed their hopes on stockpiles of antiviral agents, primarily oseltamivir, an expensive neuraminidase inhibitor. In 2005, WHO established its Southeast Asian Influenza Clinical Research Network to study neuraminidase inhibitor treatment of patients infected with viruses that possess pandemic potential (4). However, influenza virus A (H1N1) has developed resistance to oseltamivir, and similar antiviral resistance could develop in a future pandemic virus. Five million treatment courses (10 doses per patient) of oseltamivir have been donated to a WHO stockpile, but WHO has no plans to dramatically increase the size of this stockpile. On their own, the governments of a few countries that do not produce influenza vaccines or antiviral agents have purchased supplies of oseltamivir, but their stockpiles are sufficient to treat only 1% of their combined populations (D.S. Fedson, unpub. data). Not surprisingly, developing countries themselves “will not allocate scarce resources to stockpile significant quantities of oseltamivir for an unpredictable influenza pandemic” (1). Clearly, the limited supplies of antiviral agents available to developing countries where these infections now occur will scarcely have any effect on a pandemic after it starts to spread.


Thumbnail of Genetic reassortment and genesis of a new pandemic influenza virus. This study was designed to determine whether the selection and transmission of a new reassortant influenza A virus could occur under experimental conditions in vivo that mimic what might occur in nature. Reassortment between 2 antigenically distinct influenza A viruses was studied in turkeys that had been previously immunized to induce low levels of antibodies to the hemagglutinin (H) of a nonlethal turkey influenza

Figure. Genetic reassortment and genesis of a new pandemic influenza virus. This study was designed to determine whether the selection and transmission of a new reassortant influenza A virus could occur under...

Influenza virologists report that recent isolates of highly pathogenic influenza viruses (H5N1 and H7N1) have acquired molecular characteristics suggesting they might become more easily transmissible among humans (5,6). In Indonesia, physicians have reported that everyone infected with the clade 2 influenza virus A (H5N1) who did not receive antiviral treatment has died (Table 1) (7). Given extremely limited global supplies of antiviral agents, this is a terrifying observation. If a pandemic virus were to emerge with a level of virulence approaching that of influenza virus A (H5N1) in Indonesia, it could lead to a global population collapse. Many influenza virologists doubt this will ever happen and believe instead that influenza virus (H7N7) or reemergent influenza virus (H2N2) could also cause the next pandemic. Chances are they might be right. Moreover, health officials in national governments and international agencies estimate that expected pandemic deaths will be no more than what can be extrapolated from the 1918–1920 pandemic (8). These officials seldom, if ever, use the phrases “population collapse” or “population die off,” and their estimates may also be right. Nonetheless, in a seminal experiment reported in 1974, Webster and Campbell showed that genetic reassortment, the process that gave rise to pandemic viruses in 1957 and 1968, could give rise to a readily transmissible virus of extraordinary virulence (Figure) (9). This experiment and human experience with influenza virus A (H5N1) in Indonesia suggest it would be prudent for all countries to plan for something much worse than what occurred in 1918–1920.

The current approach to pandemic planning for all countries involves small groups of health officials, influenza scientists, and company executives, most of whom come from industrialized countries. For the foreseeable future, this top-down approach will be incapable of providing developing countries with timely supplies of affordable vaccines and antiviral agents. (Most industrialized countries that do not produce influenza vaccines will have similar difficulties, at least for the first pandemic wave.) The Indonesian Health Minister, for one, understands this. With little prospect that people in her country will be able to obtain vaccines against pandemic viruses, she precipitated a standoff with WHO by announcing in February 2007 that unless Indonesia is able to gain access to supplies of vaccines against pandemic viruses, her country will no longer share its influenza viruses A (H5N1) with WHO’s laboratory-based surveillance system (2). Despite unorthodox arguments (10), her position has garnered wide support from the health ministers of many developing countries (11). Recently, Indonesia agreed to share influenza virus A (H5N1) sequences (not the viruses themselves) with the Global Initiative on Sharing Avian Influenza Data, but the country no longer promptly reports deaths from influenza virus A (H5N1), in defiance of new International Health Regulations. WHO has been unable to come up with a solution to this impasse.

In identifying the major issues and challenges of a pandemic threat facing developing countries, Oshitani et al. have called for better preparedness planning, improved systems for medical care and public health, expanded use of nonpharmaceutical interventions, and strengthened core capacities for seasonal influenza surveillance and vaccination (1). They recognize that this is a challenge few developing countries will be able to meet, but go on to say, “Preparing for a pandemic by simply strengthening preparedness within a single country is not possible. A pandemic is a global issue, and pandemic preparedness should be considered from a global perspective” (1). In practical terms, what exactly does this mean? The record thus far indicates that truly international efforts to prepare for pandemic vaccination and antiviral use have been meager. In almost all instances, these efforts have been vastly outweighed by efforts that reflect national concerns and interests.

A Bottom-Up Approach that Developing Countries Can Use to Confront the Next Pandemic

A top-down approach will not ensure that adequate and affordable supplies of vaccines against pandemic viruses and antiviral agents can be produced and distributed in time to protect populations in developing countries. Transferring technology for vaccine and antiviral agent production to a small number of developing countries will proceed slowly and will inevitably fail to meet the needs of neighboring countries not favored by these programs (12). Consequently, developing countries must consider an alternative bottom-up approach to pandemic control, an approach based on existing healthcare workers and institutions and that uses inexpensive and widely available generic agents that have intrinsic antiviral activities or that modify the host response (13,14).

Many influenza scientists doubt this approach will work (1416). Nonetheless, as reviewed elsewhere (13,14), several retrospective studies suggest that outpatient statins (drugs taken to lower cholesterol levels and prevent cardiovascular diseases) reduce 30-day pneumonia mortality rates by ≈50% (Table 2) (1722). Most investigators agree that these observational studies must be interpreted with caution and that promising results should be followed by prospective clinical trials. One such trial is already under way, and a preliminary report has shown that in 67 pneumonia patients in intensive care units, treatment with statins reduced the hospital mortality rate by 51% (p = 0.026) (23). Pulmonary investigators also believe that peroxisome proliferator–activated receptor (PPAR) α and PPARγ agonists (fibrates and glitazones, respectively) could be used to treat acute lung injury (14). An important experimental study has shown that the fibrate gemfibrozil, a PPARα agonist used to prevent heart disease, reduced mortality rates in mice infected with influenza virus (H2N2) by 54% (24). Statins and PPAR agonists have antiinflammatory and immunomodulatory activities, and there is considerable molecular cross-talk between these agents (14). Moreover, combination treatment is safe, and in patients with cardiovascular diseases, clinical benefits are additive. Used either alone or together, this treatment might similarly benefit patients during an influenza pandemic.

Other generic agents, some with direct activity against influenza virus, should also be considered (14). Chloroquine, long used as an antimalarial drug, increases endosomal pH and acts as an antiviral agent by impairing virus release into the cytosol. Resveratrol, a polyphenol found in red wine, reduces influenza mortality rates in experimentally infected mice (25). Catechins (found in green tea) (26) and curcumin (turmeric; found in curry powder) (27) have numerous cell-signaling effects, suggesting that they too might be beneficial. A combination of agents that act on both the host response and the virus might be required.

It is becoming increasingly difficult for investigators to ignore arguments for treating the host response to influenza. Recently, investigators showed that giving a neuraminidase inhibitor to mice infected with influenza virus A (H5N1) was not nearly as effective as treating the mice with an antiviral agent and 2 immunomodulatory agents, mesalazine, a PPARγ agonist, and celecoxib, a cyclooxygenase (COX)–2 inhibitor (28,29). In this model, targeting the host response to infection was essential for improving survival rates and times. More important, 2 studies in mice showed that intratracheal administration of either a fragment of the PB1-F2 protein of the 1918 influenza virus (30) or an inactivated influenza virus A (H5N1) (31) caused severe acute lung injury similar to that seen in fatal human cases of influenza (either from the 1918–1920 pandemic or from the current H5N1 subtype). In these experimental models, there was no virus replication. Thus, antiviral agents would have had no effect. Although we still lack direct evidence that one or more antiinflammatory and immunomodulatory agents alone would effectively treat human influenza virus A (H5N1) infections, these results and those from the study of influenza virus (H2N2)–infected mice treated with gemfibrozil (24) suggest these agents might be effective.

What makes these agents so important is that many of them are currently being produced as generic drugs in developing countries (13,14). These drugs are inexpensive, could be produced in abundance, and could even be stockpiled and made available for use on the first day of a pandemic. No matter what is accomplished in the years ahead, adequate supplies of vaccines and specific antiviral agents will never be available to persons in developing countries on the first pandemic day.

A Research Agenda to Establish a Generic Approach to Pandemic Treatment and Prophylaxis

What types of research on generic agents do we need before the pandemic virus appears? First, experimental studies of several candidate treatment regimens must be undertaken in mice infected with influenza virus A (H5N1) or 1918-like viruses (Table 3). The agents used in these studies might have antiinflammatory and immunomodulatory or antiviral properties (some might have both), but all must be generic agents that are currently produced in developing countries. Admittedly, these experimental studies in mice will have limitations (32), but they should identify avenues for further research. Once a few treatment regimens have been shown to be effective in mice, they should be tested in ferrets. Later, 2 or 3 of the most promising regimens should be tested in nonhuman primates.

After demonstrating the effectiveness of 1 or more treatment regimens in animals, influenza virologists should then use in vitro systems to define the molecular mechanisms responsible for their protective activity. However, some of these agents will have broader effects on the host response. For example, although administering a COX-2 inhibitor along with a PPARγ agonist improved survival rates and times in mice infected with influenza virus A (H5N1) (21), another study showed that selective COX-2 inhibition was detrimental to the resolution of acute lung injury (33). Most influenza scientists focus their research on the virus or on cell-signaling events associated with viral pathogenesis (34). Yet the pathophysiologic effects of severe infections involve the entire host, something well known to researchers who study sepsis (3537). Their studies have shown that statins and PPAR agonists stabilize myocardial and microvascular function, preserve integrity of pulmonary endothelial cell tight junctions and prevent pulmonary edema, and promote resolution of acute inflammation (13,14). Thus, other investigators with laboratory and clinical expertise in critical care, cardiopulmonary diseases, and endocrinology and metabolism must be recruited to explore in animals the molecular mechanisms underlying these broad treatment effects on the host. However, in undertaking this research, investigators must not forget that their primary goal is to find effective ways to manage a pandemic in populations and not simply to explain in more precise terms the harmful effects of pandemic virus infection in individuals.

While these studies are under way, an analysis should be undertaken for each candidate agent to determine which companies produce them, where each is manufactured, annual levels of production (and surge capacity), patterns of distribution to other developing countries, and costs for public markets (Table 3). Special attention must be given to companies that follow Good Manufacturing Practices to minimize the risk that some of these agents might be counterfeit. When animal studies have defined 1 or more promising regimens, an international process must be set up to develop logistics for financing, producing, and distributing each agent.

Where feasible, clinical trials of promising treatment regimens might be undertaken in patients with severe seasonal influenza. In a few instances, clinicians might choose to treat patients infected with influenza virus A (H5N1) on a compassionate basis (12). However, none of these limited studies will guarantee that promising treatments in the prepandemic period will be effective against a true pandemic virus. Thus, careful plans must be made during the prepandemic period that will enable investigators to conduct randomized controlled trials of promising generic regimens during the early weeks of a new pandemic. If the case-fatality rate is similar to that of influenza virus A (H5N1) (≈60%), trials will not need to be large (Table 4). Within a few days, investigators should be able to recruit sufficient numbers of patients to satisfy statistical requirements.

Planning for clinical trials during the prepandemic period must start with identifying clinical investigators who will conduct these trials and institutions that will sponsor their work. Supplies of the agents to be tested must be set aside, study protocols written, and ethical approval obtained. A mechanism for rapid regulatory approval must be developed to enable trials to be conducted wherever the pandemic virus first emerges. A financing mechanism must be established that enables immediate access to funds necessary to support the trials. Finally, an internet-based communication strategy must be devised that ensures prompt dissemination of study results to physicians and health officials worldwide.

None of this research on generic agents will be possible without international coordination. Thus far, the top-down approach that has characterized vaccine and antiviral research and development has lacked an international system for coordination and management to ensure rapid progress (2). Likewise, nothing has been done to ensure worldwide production and distribution of the vaccines and antiviral agents being developed. A similar approach must not be allowed to govern the research agenda for generic agents.

Experience with the severe acute respiratory syndrome (SARS) in 2003 shows us how we could do much better. When SARS first came to international attention, WHO quickly established 3 virtual networks of experienced virologists, clinicians, and epidemiologists (38). By sharing experiences and findings on secure websites and in daily teleconferences, investigators soon identified and sequenced the SARS coronavirus, defined the clinical features of the disease, and established practical measures for clinical management and epidemiologic control. Surprisingly, WHO has not set up a similar system to coordinate research and development of vaccines against pandemic viruses and antiviral agents, despite the far greater threat to global health inherent in an influenza (H5N1) pandemic (2). Given escalating pressure from developing countries, WHO can ill afford to adopt the same slow approach to establishing the scientific basis for using inexpensive and widely available generic agents for pandemic control.


Oshitani et al. correctly emphasize that preparing for the next pandemic requires a global perspective, but this does not necessarily mean that the measures used to confront the pandemic in developing countries must be supplied through an internationally organized top-down process. An international process will surely be required for distributing vaccines and antiviral agents, but experience indicates that the process will be slow and cumbersome and supplies of these agents will remain scarce (2). Nonetheless, developing countries will need abundant supplies of effective agents, and abundance will be guaranteed only if these agents are generic, inexpensive, and produced in developing countries themselves.

It is too soon to know whether generic agents could be used to confront the next influenza pandemic, yet developing countries lack realistic alternatives. For this reason, their leaders must convince scientists and international organizations, including WHO, of the urgent need for research to determine whether these inexpensive agents could mitigate the effects of a pandemic. Otherwise, developing and industrialized countries alike could be faced with an unprecedented global health crisis.

Dr Fedson is a former professor of medicine at the University of Virginia and former Director of Medical Affairs in Europe for Aventis Pasteur MSD (now Sanofi Pasteur MSD). Since retiring in 2002, he has continued to write and lecture about influenza vaccination, pandemic preparedness, and the potential for using generic agents for pandemic treatment and prophylaxis.



The author thanks Charles Liss for calculating sample sizes (Table 4) and Astutie Michel for preparing the figure.



  1. Oshitani  H, Kamigaki  T, Suzuki  A. Major issues and challenges of influenza pandemic preparedness in developing countries. Emerg Infect Dis. 2008;14:87580. DOIPubMedGoogle Scholar
  2. Fedson  DS, Dunnill  P. From scarcity to abundance: pandemic vaccines and other agents for “have not” countries. J Public Health Policy. 2007;28:32240. DOIPubMedGoogle Scholar
  3. World Health Organization. Options for the use of human H5N1 influenza vaccines and the WHO H5N1 vaccine stockpile. WHO scientific consultation. 2007 Oct 1–3; Geneva [cited 2008 Dec 10]. Available from
  4. Higgs  ES, Hayden  FG, Chotpitayasunondh  T, Whitworth  J, Farrar  J. The Southeast Asian Influenza Clinical Research Network: development and challenges for a new multilateral research endeavor. Antiviral Res. 2008;78:648. DOIPubMedGoogle Scholar
  5. Chen  LM, David  CT, Zhou  H, Cox  NJ, Donis  RO. Genetic compatibility and virulence of reassortants derived from contemporary avian H5N1 and human H3N2 influenza A viruses. PLoS Pathog. 2008;4:e1000072. DOIPubMedGoogle Scholar
  6. Belser  JA, Blixt  O, Chen  LM, Pappas  C, Maines  TR, Van Hoeven  N, Contemporary North America influenza H7 viruses possess human receptor specificity: implications for virus transmissibility. Proc Natl Acad Sci U S A. 2008;105:755863. DOIPubMedGoogle Scholar
  7. Reports of increased survival in bird flu patients taking Tamiflu. International Symposium on Respiratory Viral Infections; 2008 Mar 2; Singapore [cited 2008 Dec 10]. Available from
  8. Murray  CJL, Lopez  AD, Chin  B, Feehan  D, Hill  KH. Estimation of potential global influenza mortality on the basis of vital registry data from the 1918–1920 pandemic: a quantitative analysis. Lancet. 2006;368:22118. DOIPubMedGoogle Scholar
  9. Webster  RG, Campbell  CH. Studies on the origin of pandemic influenza. IV. Selection and transmission of “new” influenza viruses in vivo. Virology. 1974;62:40413. DOIPubMedGoogle Scholar
  10. Fidler  DP. Influenza virus samples, international law, and global health diplomacy. Emerg Infect Dis. 2008;14:8894. DOIPubMedGoogle Scholar
  11. Schnirring  L. Indonesia claims wide support for virus-sharing stance. Center for Infectious Disease and Research Policy News. 2008 May 27 [cited 2008 Dec 12]. Available from
  12. Fedson  DS. New technologies for meeting the global demand for pandemic influenza vaccines. Biologicals. 2008;36:3469. DOIPubMedGoogle Scholar
  13. Fedson  DS. Pandemic influenza: a potential role for statins in treatment and prophylaxis. Clin Infect Dis. 2006;43:199205. DOIPubMedGoogle Scholar
  14. Fedson  DS. Confronting an influenza pandemic with inexpensive generic agents: can it be done? Lancet Infect Dis. 2008;8:5716. DOIPubMedGoogle Scholar
  15. Butler  D. Cheaper approaches to flu divide flu researchers. Nature. 2007;448:9767. DOIPubMedGoogle Scholar
  16. Writing Committee of the Second World Health Organization Consultation on Clinical Aspects of Human Infection with Avian Influenza A (H5N1) Virus; Abdel-Ghafar AN, Chotpitayasunondh T, Gao Z, Hayden FG, Nguyen DH, de Jong MD, et al. Update on avian influenza A (H5N1) virus infection in humans. N Engl J Med. 2008;358:261–73.
  17. van de Garde  EM, Hak  E, Souverein  PC, Hoes  AW, van den Bosch  JM, Leufkens  HG. Statin therapy and reduced risk of pneumonia in patients with diabetes. Thorax. 2006;61:95761. DOIPubMedGoogle Scholar
  18. Schlienger  RG, Fedson  DS, Jick  S, Jick  H, Meier  C. Statins and the risk of pneumonia: a population-based nested case-control study. Pharmacotherapy. 2007;27:32532. DOIPubMedGoogle Scholar
  19. Mortensen  EM, Pugh  MJ, Copeland  L, Cornell  J, Restrepo  MI, Anzueto  A, Impact of statins and ACE inhibitors on mortality for patients hospitalized with community-acquired pneumonia and influenza. Eur Respir J. 2008;31:6117. DOIPubMedGoogle Scholar
  20. Chalmers  JD, Singanayagam  A, Murray  MP, Hill  AT. Prior statin use is associated with improved outcomes in community-acquired pneumonia. Am J Med. 2008;121:10027. DOIPubMedGoogle Scholar
  21. Thomsen  RW, Riis  A, Kornum  JB, Christensen  S, Johnsen  SP, Sorensen  HT. Preadmission use of statins and outcomes after hospitalization with pneumonia. Arch Intern Med. 2008;168:20817. DOIPubMedGoogle Scholar
  22. Majumdar  SR, McAlister  FA, Eurich  DT, Padwal  RS, Marrie  TJ. Statins and outcomes in patients admitted to hospital with community acquired pneumonia: a population based prospective cohort study. BMJ. 2006;333:9991004. DOIPubMedGoogle Scholar
  23. Choi  HS, Park  MJ, Kang  HM, Lim  IH, Choi  CW, You  JH. Statin use and mortality in sepsis due to pneumonia. Crit Care Med. 2007;35(Suppl):1362. DOIPubMedGoogle Scholar
  24. Budd  A, Alleva  L, Alsharifi  M, Koskinen  A, Smytha  V, Mullbacher  A, Increased survival after gemfibrozil treatment of severe mouse influenza. Antimicrob Agents Chemother. 2007;51:29658. DOIPubMedGoogle Scholar
  25. Palamara  AT, Nencioni  L, Aquilano  K, De Chiara  G, Hernandez  L, Cossolino  F, Inhibition of influenza A virus replication by resveratrol. J Infect Dis. 2005;191:171929. DOIPubMedGoogle Scholar
  26. Song  JM, Park  KD, Lee  KH, Byun  YH, Park  JH, Kim  SH, Biological evaluation of anti-influenza viral activity of semi-synthetic catechin derivatives. Antiviral Res. 2007;76:17885. DOIPubMedGoogle Scholar
  27. Siddiqui  AM, Cui  X, Wu  R, Dong  W, Zhou  M, Hu  M, The anti-inflammatory effect of curcumin in an experimental model of sepsis is mediated by up-regulation of peroxisome proliferator-activated receptor-gamma. Crit Care Med. 2006;34:187482. DOIPubMedGoogle Scholar
  28. Zheng  BJ, Chan  KW, Lin  YP, Zhao  GY, Chan  C, Zhang  HJ, Delayed antiviral plus immunomodulator treatment still reduces mortality in mice infected by high inoculum of influenza A/H5N1 virus. Proc Natl Acad Sci U S A. 2008;105:80916. DOIPubMedGoogle Scholar
  29. Simmons  C, Farrar  JT. Insights into inflammation. N Engl J Med. 2008;359:16213. DOIPubMedGoogle Scholar
  30. McAuley  JL, Hornung  F, Boyd  KL, Smith  AM, McKeon  R, Bennick  J, Expression of the 1918 influenza A virus PB1–F2 enhances the pathogenesis of viral and secondary bacterial pneumonia. Cell Host Microbe. 2007;2:2409. DOIPubMedGoogle Scholar
  31. Imai  Y, Kuba  K, Neely  GG, Yaghubian-Malhami  R, Perkmann  T, van Loo  G, Identification of oxidative stress and Toll-like receptor 4 signaling as a key pathway of acute lung injury. Cell. 2008;133:23549. DOIPubMedGoogle Scholar
  32. Mizgerd  JP, Skerrett  SJ. Animal models of human lung disease. Am J Physiol Lung Cell Mol Physiol. 2008;294:L38798. DOIPubMedGoogle Scholar
  33. Fukunaga  K, Kohli  P, Bonnans  C, Fredenburgh  LE, Levy  BD. Cyclooxygenase 2 plays a pivotal role in the resolution of acute lung injury. J Immunol. 2005;174:50339.PubMedGoogle Scholar
  34. Korteweg  C, Gu  J. Pathology, molecular biology, and pathogenesis of avian influenza A (H5N1) infection in humans. Am J Pathol. 2008;172:115570. DOIPubMedGoogle Scholar
  35. van der Poll  T, Opal  SM. Host-pathogen interactions in sepsis. Lancet Infect Dis. 2008;8:3243. DOIPubMedGoogle Scholar
  36. Rittirsch  D, Flierl  MA, Ward  PA. Harmful molecular mechanisms in sepsis. Nat Rev Immunol. 2008;8:77687. DOIPubMedGoogle Scholar
  37. Carré  JE, Singer  M. Cellular energetic metabolism in sepsis: the need for a systems approach. Biochim Biophys Acta 2008;1777:763–71.
  38. World Health Organization. WHO global conference on severe acute respiratory syndrome (SARS). Where do we go from here? 2003 Jun 17–18 [cited 2008 Dec 10]. Available from




Cite This Article

DOI: 10.3201/eid1503.080857

Table of Contents – Volume 15, Number 3—March 2009

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.



Please use the form below to submit correspondence to the authors or contact them at the following address:

David S. Fedson, 57 Chemin du Lavoir, 01630 Sergy Haut, France

Send To

10000 character(s) remaining.


Page created: December 07, 2010
Page updated: December 07, 2010
Page reviewed: December 07, 2010
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.