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Medicine » Infectious Diseases » "Clinical Management of Complicated Urinary Tract Infection", book edited by Ahmad Nikibakhsh, ISBN 978-953-307-393-4, Published: September 6, 2011 under CC BY-NC-SA 3.0 license. © The Author(s).

Chapter 11

Rheumatoid Arthritis is Caused by Asymptomatic Proteus Urinary Tract Infections

By Taha Rashid and Alan Ebringer
DOI: 10.5772/24417

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Rheumatoid Arthritis is Caused by Asymptomatic Proteus Urinary Tract Infections

Taha Rashid1 and Alan Ebringer1

1. Introduction

Urinary tract infections (UTI) are considered as one of the most common groups of infections in humans and affecting either the upper (kidneys--pyelonephritis) or the lower (bladder--cystitis) part of the urinary tract (Thomson and Armitage, 2010).

The gastrointestinal tract is a reservoir from which uropathogens emerge. Reflecting this, Enterobacteriaceae are the most important cause of UTI in all population groups, accounting for more than 95% of all UTIs. Among these microbes, E. coli is by far the most common invader, causing some 90% of UTIs in outpatients and approximately 50% in hospitalized patients. Whilst, the frequency of P. mirabilis causing outpatient and inpatients UTIs were 3.2% and 12.7% respectively, these value were reversed to 26.6% and 9.3% when all strains of Proteus species were examined (Talkoff-Robin et al, 2008). In a most recent multicentre study involving nine Spanish hospitals, 784 women with uncomplicated cystitis were evaluated for the frequencies of isolated uropathogens and their susceptibility to antibiotics. Among the 650 pathogens isolated, the first group of the most frequent bacterial agents was Escherichia coli (79.2%) followed by Staphylococcus saprophyticus (4.4%), Proteus mirabilis (4.3%), Enterococcus faecalis (3.3%), and Klebsiella pneumoniae (2.3%) (Palou et al, 2011).

In contrast to E. coli strains, it appears that all strains of P. mirabilis, regardless of isolate origin, are capable of infecting the urinary tract (Sosa et al, 2006). Proteus is particularly significant as a renal pathogen especially in causing upper UTI because of its propensity to promote struvite renal calculi (Ronald and Nicolle, 2007).

2. Asymptomatic bacteriuria and subclinical urinary infections

Bacteriuria might be either symptomatic or asymptomatic. An estimated 40% of women and 12% of men will experience at least one attack of symptomatic or overt UTI during their lifetime, and approximately a quarter of affected women will suffer recurrent UTIs within 6-12 months (Nielubowicz and Mobley, 2010).

Asymptomatic bacteriuria (ABU) is considered as one of the most common findings in women all over the world. It is defined as the presence of ≥105 cfu/ml of the same bacterial species in two consecutive midstream urine samples (Schmiemann et al, 2010). Although in the majority of patients with ABU the site of infection is in the lower urinary tract, some individuals with ABU, however, do have upper tract involvement (Ronald and Nicolle, 2007). In a cross-sectional longitudinal study, Kunin and associates have found that among 16,000 schoolgirls with ages ranging between 6 to 18 years the prevalence of UTI was 1.2%, and two-third of 5% girls who had one or more episodes of bacteriuria were asymptomatic (Kunin, 1970). It also appears that the prevalence of asymptomatic bacteriuria increases with age and this has been reported by Gaymans et al (1976), where in a study of 1,758 Dutch women, the prevalence of bacteriuria was found to be increased from 2.7% of women aged 15 to 24 years to 9.3% of women aged 65 years or older.

Although it is usually true to say that bacteriuria is a valid indicator of either bacterial localization or infection of the urinary tract, studies in animals (Mulvey et al, 1998) and humans (Elliott et al, 1985) have indicated that bacteria may reside in the urothelium in the absence of bacteriuria. The majority of patients with kidney or upper tract infection show the clinical signs and symptoms of pyelonephritis, but in others this might not be the case. In a study by Stamey et al (1965), using ureteral catheterization it was shown that 50 percent of women with asymptomatic bacteriuria had infection in their upper tracts, and that a small but significant proportion of women with preliminary associated cystitis also had upper UTI. It is possible that bacteria within the kidney or upper urinary tract may remain latent in a nidus of infection for any length of time (Cattell, 2005). For example Proteus spp. can form urinary calculi and remain dormant inside these infected stones undetected and resistant to the effects of antibiotics used. It should also be stressed that P. mirabilis is probably the second most common microbe among the family of Enterobacteriaceae after E. coli in causing UTI, especially of the upper tract in middle-aged and elderly women (Senior, 1979).

3. Rheumatoid arthritis and urinary tract infections

Rheumatoid arthritis (RA) is a potentially disabling chronic systemic polyarthropathy with a world-wide distribution and an increased likelihood to have a considerable amount of negative impacts on the economical status of the patient and society (Zhang and Anis 2011). The cause of this disease is generally agreed to be due to a combined action of genetic and environmental (mainly microbial) factors (Firestein, 2009).

Among the urologists and rheumatologists, the evidence of the link between UTIs and RA is not apparently recognized because of the consistent lack of data supporting this association and more probably because of the possibility for an existing hidden infection expressed in the form of asymptomatic bacteriuria in patients with RA.

In a preliminary study carried out by a group from Tel Aviv, it has been found that 35 percent of patients with RA and secondary Sjogren’s syndrome had recurrent attacks of UTIs (Tishler et al, 1992). Furthermore, another group from Edinburgh, using a necroscopic examination of kidneys from dead patients with RA, found that approximately 17.6 percent of males and 22.7 percent of female patients showed signs of chronic pyelonephritis (Lawson and Maclean, 1966). A similar result was found in a previous study carried out by a group from Copenhagen, where a considerably high degree of associated non-obstructive pyelonephritis and renal papillary necrosis was detected among the renal autopsy materials from patients with RA (Clausen and Pedersen, 1961). However, this kind of association between RA and UTIs was not always observed (Vandenbroucke et al, 1987). This discrepancy in the results with an apparent lack of the epidemiological link between urinary infections and RA could be due to the occurrence of sub-clinical or occult infections, which are merely characterized by bacteriuria.

4. Proteus in the urine of patients with RA

RA is most probably caused or initiated by an upper urinary tract infection with Proteus bacteria. Regarding this particular subject, more than 100 articles have been published by our and various other collaborative as well as independent groups throughout the world (Ebringer et al, 2010).

The first evidence of a link between Proteus microbe and RA was reported nearly three decades ago where in a study by Chandler and co-workers, it was shown that among a panel of 30 microbial agents tested, the mean geometric titres of antibodies were raised only against Proteus OXK and herpes virus hominis microbes in 22 newly diagnosed RA patients when compared to 22 control subjects (Chandler et al, 1971). Meanwhile, this disease-microbe association was established fourteen years later in a study by our group, where a significant elevation of Proteus antibodies (p<0.001) was shown in 30 patients with RA compared to 41 healthy controls (Ebringer et al, 1985). To search for the source of this microbe in urinary tract of RA patients various studies were carried out by our and other independent groups:

  1. In a controlled study of 89 patients with RA from London, P. mirabilis was isolated from the urine of 63% of female and 50% of male patients and these results were found to be significant in comparison to female (32%) (p<0.001) or male (11%) (p<0.001) healthy subjects. However, the frequency of the isolation of Proteus from urine of men and women patients without RA (osteoarthritis, fibromyalgia, psoriasis, gout, and systemic lupus erythematosus) was 7% and 35% respectively, which were similar to those obtained from healthy men (11%) and women (32%) individuals (Figure 1). Furthermore, a positive correlation was found between high anti-Proteus antibody levels in sera of RA patients and the number of colony-forming units obtained from urine specimens of these patients (Wilson et al, 1997).

  2. In another study carried out by a group of scientists from Dundee in the UK, a significantly increased isolation rate of Proteus microbes from the urine of 76 patients (33%) were detected when compared to those of 48 gender-matched healthy individuals (4%) (Senior et al 1999) and this isolation rate was found to be occurring twice more frequently as E. coli. In the same study significant elevations (p<0.001) of antibodies against P. mirabilis were detected in the urine and serum samples of patients with RA when compared to the corresponding healthy subjects.

Another group, however, was unable to find a significant increase in the isolation of Proteus microbes from the urine or faeces of RA patients (McDonagh et al, 1994).

5. Proteus virulence factors and cross-reactive antigens

The main virulence factors which have been involved in the uropathogenetic mechanisms and utilized by the major group of uropathogens, namely E. coli and P. mirabilis include motility, adherence, biofilm formations, β-lactamase productions, toxin productions, hydrolytic enzyme productions, metal acquisitions and evasion of the host immune defenses (Dobrindt, 2010).


Figure 1.

Percentage isolation of Proteus bacteria from the urine of rheumatoid arthritis (RA) and non-RA patients and healthy controls. (Urine cultures were measured down to the level of 1 cfu/ml of urine, to determine presence or absence of bacterial signal).

In contrast to E. coli, P. mirabilis is the main producer of the urease enzyme (Rozaliski et al, 1997), which hydrolyzes urea into ammonia and carbonate. One of the hallmarks of UTI caused by P. mirabilis is the production of urinary stones through action of urease. These stones which are a composite of magnesium ammonium phosphate crystals (struvite), might act as infective reservoirs of Proteus microbes, and basically protected from host defenses and antibiotic treatment (Li et al, 2002).

Proteus microbes possess various different antigens. Two of these were found to resemble self tissue antigens. The Proteus haemolysin protein possesses six amino acid molecules “ESRRAL” which resembles a similar amino acid motif “EQRRAA” present in the HLA-DR1/4 genetic molecules (Wilson et al, 1995) frequently found in association with RA (Stastny, 1976). Whilst another group of antigens comprising five amino acid molecules “IRRET” which is present in Proteus urease resembles the “LRREI” motif present in type XI collagens (Wilson et al, 1995), which is found in hyaline cartilage of the joint tissues.

6. Proteus antibodies and their role in the pathogenetic mechanism of RA

Elevated levels of antibodies to P. mirabilis have been detected in patients with RA among many populations from 14 different countries including UK, USA, France, and Netherlands (Ebringer et al, 2010). These results have been detected by using various immunological methods carried out by collaborative (Table 1) and other independent (Tables 2) groups. The specificity of Proteus antibodies in patients with RA was shown in many studies. Deighton et al, found that antibodies to P. mirabilis but not to four different viruses (Deighton1 et al, 1992) were elevated significantly in RA patients. Moreover, in a review analysis it was shown that in patients with RA there were significant elevations of antibodies to Proteus but not against more than 20 other enterobacterial or uropathogenic microbes, including E. coli (Rashid et al, 2007).

As the result of molecular mimicry or similarity between Proteus and self antigens, patients infected with Proteus microbes will produce not only antibodies against this microbe but also against the self tissue molecules carrying the cross-reactive antigens. These antibodies will bind to and be cytopathic to the joint tissues which carry Proteus cross-reactive antigens (Wilson et al, 2003) and this immune reaction will lead to the release of more self tissue antigens with a consequent production of further autoantibodies, propagation of the pathological process and the development of classical RA, in the same way that Streptococcus causes rheumatic fever and valvular lesions in the heart (Guilherme et al, 2011).

7. A proposal for a new treatment in RA—eradication of Proteus microbes

Currently the pharmacologic treatment of RA mainly involves the use of disease modifying anti-rheumatic drugs and biological agents (Haraoui and Pope, 2011). In concurrent use with these medical treatments other therapeutic measures can be employed in order to eradicate Proteus bacteria from the urinary tract which could help to prevent further tissue and joint damages in patients with RA. These measures could involve the use of cranberry juice products, antibiotics or even vaccination.

Cranberry products have been used widely for several decades for the prevention and treatment of UTIs. A meta-analysis has established that recurrence rates of UTIs over 1 year are reduced approximately by 35% in young to middle-aged women (Guay, 2009). Other studies, however, either supported (Ferrara et al, 2009) or disputed (Barbosa-Cesnik et al, 2011) the effect of cranberry preparations in the prevention of UTIs.

Although the use of anti-microbial agents has not been recognized in the management of RA, some antibiotics have already been tried with encouraging results. Among these are sulphasalazine, metronidazole, rifampicin and minocycline (Ebringer et al, 2003). Some problems, however, exist in regard to the use of antibiotics against Proteus microbes. Firstly, Proteus infection affects mainly the kidneys and upper urinary tract (Fairley, et al, 1971) where the use of ordinary sterilizing substances and antibiotics can be less effective. Secondly, P. mirabilis possesses various virulence factors which enhance its urinary epithelial invasiveness rendering this microbe resistant to antibiotics (Mathoera et al, 2002). Thirdly, when an infected struvite stone is present in the kidney, none of the antibiotic agents seems to be effective unless the stone is removed by surgery or shock-wave therapy.

In order to test the effects of antibiotics in patients with RA through prospective longitudinal studies, the search for an effective anti-Proteus chemotherapeutic agent is mandatory. In a most recent study from Japan it was shown that all of the P. mirabilis strains including extended system β-lactamase (ESBL)-producing strains were susceptible to penicillin derivatives combined with β-lactamase inhibitors (Ishikawa et al, 2011). In another study, it was shown that among the three carbapenems tested, meropenem was the most potent antibiotic being effective against the majority of the Proteus species isolates (Lee et al, 2011). If patients with RA respond to anti-microbial measures, prophylaxis of susceptible individuals could be instigated by the mean of immunization with attenuated antigens from causative microbe or other cross-reactive microbes among the Enterobacteriaceae group (Scavone et al, 2011).

It is logical to start treating patients with RA from early stages of the disease in order to prevent further irreversible joint damages from occurring. If such early therapy is undertaken the possibility arises that RA may be eradicated in the same way that rheumatic fever has been eliminated in the Western World by the means of early treatment of Streptoccocal tonsillitis with penicillin and other related antibiotics.

8. General discussion

It generally appears that there is an apparent relationship between Proteus asymptomatic UTIs and RA. The main hallmark of this association is based on showing the linkage between RA and Proteus but not other microbes in the majority of studies carried out by various groups throughout the world. The combination of isolation of Proteus microbes in the urine and elevation of antibodies in sera of RA patients as well as the evidence for the cytopathic effects of these antibodies against the joint tissue cross-reactive antigens, forms the major evidence for the role of this microbe in the development of RA. Elimination of Proteus microbes by using cranberry juice, antibiotics could have a remarkable effect in the management of RA patients alongside currently used anti-rheumatic drugs. It would appear that the management of RA may be relevant to urologists as well as to rheumatologists.

19853041AMP<0.001Ebringer et al
19883218ELISAP<0.05Khalafpour et al
19955049ELISAP<0.001Fielder et al
19954030ELISAP<0.001Wilson et al
19953433ELISA+IIFP<0.001Subair et al
19966660ELISAP<0.001Tiwana et al
19975050ELISAP<0.001Tani et al
199789234ELISAP<0.001Wilson et al
19976060ELISAP<0.001Tiwana et al
19982534IIFP<0.001Blankenberg-Sprenkels et al
199911469IIFP<0.001Rashid et al
20035138ELISAP<0.001Wilson et al
200415953IIFP<0.001Rashid et al
20065038ELISAP<0.0001Rashid et al
20077020ELISAP<0.001Rashid et al

Table 1.

RA = rheumatoid arthritis; HC = healthy controls; AM = agglutination method ; ELISA = enzyme-linked immunosorbent assay; IIF = indirect immunofluorescence.

Studies carried out by various collaborative groups showing increased anti-Proteus antibodies in patients with RA compared to HC individuals (number of subjects indicated in each study).

19882930ELISAP<0.01Rogers et al
1991910+10 (AS+HC)ELISAp<0.01; NSMurphy et al
1992142121IIFP<0.0001Deighton2 et al
19948729 (non-RA)IIFP<0.003McDonagh et al
1995 2727 (non-RA)ELISA; IBP<0.0001Senior et al
19964040ELISAP<0.001Dybwad et al
19977082AMP<0.001Wanchu et al
19993951ELISAp<0.001Chou et al
20035025AMP<0.001Gautam et al
20055963IBP<0.01Weisbart et al
200524643+90 (SpA+UA)ELISAP<0.0003; p<0.015Newkirk et al

Table 2.

*Controls are always healthy individuals unless otherwise stated; RA = rheumatoid arthritis; AS = ankylosing spondylitis; HC = healthy control; SpA = spondyloarthropathy; UA = undifferentiated arthritis; ELISA = enzyme-linked immunosorbent assay; IIF = indirect immunofluorescence; AM = agglutination method; IB = immunoblot; NS = not significant.

Studies carried out by independent groups showing increased anti-Proteus antibodies in patients with RA compared to controls.


This work was supported by the “American Friends of King’s College”.


1 - C. Barbosa-Cesnik, M. B. Brown, M. Buxton, L. Zhang, J. De Busscher, B. Foxman, 2011Cranberry juice fails to prevent recurrent urinary tract infection: results from a randomized placebo-controlled trial. Clin Infect Dis;52 23 30
2 - S. H. Blankenberg-Sprenkels, M. Fielder, T. E. Feltkamp, H. Tiwana, C. Wilson, A. Ebringer, 1998Antibodies to Klebsiella pneumoniae in Dutch patients with ankylosing spondylitis and acute anterior uveitis and to Proteus mirabilis in rheumatoid arthritis. J Rheumatol;25:743−747.
3 - Cattell WR. 2005Lower and upper urinary tract infections. In: Davison AM, Cameron JS, Grunfeld J, Ponticelli C, Ritz E, Winearls CG, van Ypersele C (editors). Oxford Textbook of Clinical Nephrology. Oxford University Press, Oxford,;1111 1129
4 - R. W. Chandler, H. Robinson, A. T. Masi, 1971Serological investigations for evidence of an infectious aetiology of rheumatoid arthritis. Ann Rheum Dis;30 274 278
5 - C. T. Chou, J. Uksila, P. Toivanen, 1998Enterobacterial antibodies in Chinese patients with rheumatoid arthritis and ankylosing spondylitis. Clin Exp Rheumatol;16 161 164
6 - E. Clausen, J. Pedersen, 1961Necrosis of the renal papillae in rheumatoid arthritis. Acta Med Scand;170 631 633
7 - Deighton1 CM, Gray JW, Bint AJ, Walker DJ. 1992Specificity of the Proteus antibody response in rheumatoid arthritis. Ann Rheum Dis;51 1206 1207
8 - Deighton2 CM, Gray JW, Bint AJ, Walker DJ. 1992Anti-Proteus antibodies in rheumatoid arthritis same-sexed sibships. Br J Rheumatol;31 241 245
9 - U. Dobrindt, 2010Virulence factors of uropathogens. Urologe A;49 598 605
10 - A. Dybwad, O. Forre, M. Sioud, 1996Increased serum and synovial fluid antibodies to immunoselected peptides in patients with rheumatoid arthritis. Ann Rheum Dis;55 437 441
11 - A. Ebringer, T. Ptaszynska, M. Corbett, C. Wilson, Y. Macafee, H. Avakian, P. Baron, D. C. James, 1985Antibodies to Proteus in rheumatoid arthritis. Lancet;ii:305 307
12 - A. Ebringer, T. Rashid, C. Wilson, 2003Rheumatoid arthritis: proposal for the use of anti-microbial therapy in early cases. Scand J Rheumatol;32 2 11
13 - A. Ebringer, T. Rashid, C. Wilson, 2010Rheumatoid arthritis, Proteus, anti-CCP antibodies and Karl Popper. Autoimm Rev;9 216 223
14 - T. S. Elliott, L. Reed, R. C. Slack, M. C. Bishop, 1985Bacteriology and ultrastructure of the bladder in patients with urinary tract infections. J Infect;11 191 199
15 - K. F. Fairley, N. E. Carson, R. C. Gutch, P. Leighton, A. D. Grounds, E. C. Laird, et al. 1971Site of infection in acute urinary tract infection in general practice. Lancet;ii:615 618
16 - P. Ferrara, L. Romaniello, O. Vitelli, A. Gatto, M. Serva, L. Cataldi, 2009Cranberry juice for the prevention of recurrent urinary tract infections: a randomized controlled trial in children. Scand J Urol Nephrol;43 369 372
17 - M. Fielder, H. Tiwana, P. Youinou, P. Le Goff, R. Deonarian, C. Wilson, et al. 1995The specificity of the anti-Proteus antibody response in tissue-typed rheumatoid arthritis (RA) patients from Brest. Rheumatol Int;15 79 82
18 - Firestein GS. 2009Etiology and pathogenesis of rheumatoid arthritis. In: Firestein GS, Budd RC, Harris Jr ED, McInnes IB, Ruddy S, Sergent JS (editors). Kelly’s Textbook of Rheumatology. Saunders-Elsevier, Philadelphia,;1035 1380
19 - V. Gautam, R. Sehgal, S. G. Paramjeet, D. R. Arora, 2003Detection of anti-Proteus antibodies in sera of patients with rheumatoid arthritis. Indian J Pathol Microbiol;46 137 141
20 - R. Gaymans, MJ Valkenburg. H. A. Haverkorn, W. R. Goslings, 1976A prospective study of urinary tract infections in a Dutch general practice. Lancet;ii:674 677
21 - Guay DR. 2009Cranberry and urinary tract infections. Drugs;69;775 807
22 - L. Guilherme, K. F. Kohler, J. Kalil, 2011Rheumatic heart disease: mediation by complex immune events. Adv Clin Chem;53 31 50
23 - B. Haraoui, J. Pope, 2011Treatment of early rheumatoid arthritis: concepts in management. Semin Arthritis Rheum;40 371 388
24 - K. Ishikawa, T. Matsumoto, M. Yasuda, S. Uehara, T. Muratani, M. Yagisawa, et al. 2011The nationwide study of bacterial pathogens associated with urinary tract infections conducted by the Japanese Society of Chemotherapy. J Infect Chemother;17 126 138
25 - S. Khalafpour, A. Ebringer, I. Abuljadayel, M. Corbett, 1988Antibodies to Klebsiella and Proteus microorganisms in ankylosing spondylitis and rheumatoid arthritis patients measured by ELISA. Br J Rheumatol;27 (Suppl. II):86 89
26 - Kunin CM. 1970The natural history of recurrent bacteriuria in schoolgirls. N Engl J Med:282 1443 1448
27 - AA Maclean. N. Lawson, 1966Renal disease and drug therapy in rheumatoid arthritis. Ann Rheum Dis;25 441 449
28 - H. Lee, K. S. Ko, J. H. Song, K. R. Peck, 2011Antimicrobial activity of doripenem and other carbapenems against gram-negative pathogens from Korea. Microb Drug Resist;17 37 45
29 - X. Li, H. Zhao, C. V. Lockatell, C. B. Drachengberg, D. E. Johnson, H. L. Mobley, 2002Visualization of Proteus mirabilis within the matrix of urease-induced bladder stones during experimental urinary tract infection. Infect Immun;70 389 394
30 - Mathoera RB, Kok DJ, Verduin CM, Nijman RJ. 2002Pathological and therapeutic significance of cellular invasion by Proteus mirabilis in an enterocystoplasty infection stone model. Infect Immun;70 7022 7032
31 - J. Mc Donagh, J. Gray, H. Sykes, D. J. Walker, A. J. Bint, C. M. Deighton, 1994Anti-Proteus antibodies and Proteus organisms in rheumatoid arthritis: a clinical study. Br J Rheumatol;33 32 35
32 - MA Lopez. Mulvey-Boado, Y. S. Wilson, C. L. Roth, R. Parks, W. C. Heuser, J. Hulgren, S. J. , 1998Induction and evasion of host defenses by type 1-pillated uropathogenic Escherichia coli. Science;282 1494 1497
33 - E. A. Murphy, L. Mowat, R. D. Sturrock, 1991Antibodies to Proteus in rheumatoid arthritis. Br J Rheumatol;30:390.
34 - MM Goldbach. Newkirk-Mansky, R. Senior, B. W. Klippel, J. Schumacher, H. R. Jr El -Gabalawy, H. S. , 2005Elevated levels of IgM and IgA antibodies to Proteus mirabilis and IgM antibodies to Escherichia coli are associated with early rheumatoid factor (RF)-positive rheumatoid arthritis. Rheumatology;44 1433 1441
35 - Nielubowicz GR, Mobley HR. 2010Host-pathogen interactions in urinary tract infection. Nat Rev Urol;7 430 441
36 - J. Palou, C. Pigrau, I. Molina, J. M. Ledesma, J. Angulo, 2011Etiology and sensitivity of uropathogens identified in uncomplicated lower urinary tract infections in women (ARESC Study): implications on empiric therapy. Med Clin (Barc);136 1 7
37 - T. Rashid, G. Darlington, J. Kjeldsen-Kragh, O. Forre, A. Collado, A. Ebringer, 1999 Proteus IgG antibodies and C-reactive protein in English, Norwegian and Spanish patients with rheumatoid arthritis. Clin Rheumatol;18 190 195
38 - T. Rashid, M. Leirisalo-Repo, Y. Tani, S. Hukuda, S. Kobayashi, C. Wilson, S. Bansal, A. Ebringer, 2004Antibacterial and antipeptide antibodies in Japanese and Finnish patients with rheumatoid arthritis. Clin Rheumatol;23 134 141
39 - T. Rashid, A. Ebringer, C. Wilson, S. Bansal, L. Paimela, A. Binder, 2006The potential use of antibacterial peptide antibody indices in the diagnosis of rheumatoid arthritis and ankylosing spondylitis. J Clin Rheumatol;12 11 16
40 - T. Rashid, A. Ebringer, 2007Rheumatoid arthritis is linked to Proteus-the evidence. Clin Rheumatol;26 1036 1043
41 - P. Rogers, J. Hassan, B. Bresnihan, C. Feighery, A. Whelan, 1988Antibodies to Proteus in rheumatoid arthritis. Br J Rheumatol;27 (Suppl.2):90-94.
42 - Ronald AR, Nicolle LE. 2007Infections of the upper urinary tract. In: Schrier RW (editor). Diseases of the Kidney and Urinary Tract. Wolters Kluwer|Lippincott Williams & Wilkins, Philadelphia: 847 869
43 - A. Rozalski, Z. Sidorczyk, K. Kotelko, 1997Potential virulence factors of Proteus bacilli. Microbiol Mol Biol Rev;61 65 89
44 - P. Scavone, A. Umpierrez, D. J. Maskell, P. Zunino, 2011Nasal immunization with attenuated Salmonella typhimurium expressing an MrpA-TetC fusion protein significantly reduced Proteus mirabilis colonization in the mouse urinary tract. J Med Microbiol; Mar 17: [Epub ahead of print].
45 - G. Schmiemann, E. Kniehl, K. Gebhardt, MM Hummers. Matejczyk-Pradier, E. , 2010The diagnosis of urinary tract infection: a systematic review. Dtsch Arztebl Int;107 361 367
46 - Senior BW. 1979The special affinity of particular types of Proteus mirabilis for the urinary tract. J Med Microbiol;12 1 8
47 - Senior BW, McBride PDP, Morley KD, Kerr MA. 1995The detection of raised levels of IgM to Proteus mirabilis in sera from patients with rheumatoid arthritis. J Med Microbiol;43 176 84
48 - Senior BW, Anderson GA, Morley KD, Kerr MA. 1999Evidence that patients with rheumatoid arthritis have asymptomatic ′non-significant’ Proteus mirabilis bacteriuria more frequently than healthy controls. J Infect;38 99 106
49 - Stamey TA, Govan DE, Palmer JM. 1965The localization and treatment of urinary tract infection: the role of bactericidal urine levels as opposed to serum levels. Medicine (Baltimore);44 1 36
50 - P. Stastny, 1976Mixed lymphocyte cultures in rheumatoid arthritis. J Clin Invest;57 1148 1157
51 - Subair H, Tiwana H, Fielder M, Binder A, Cunningham K, Ebringer A et al. 1995 Elevation in anti-Proteus antibodies in patients with rheumatoid arthritis from Bermuda and England. J Rheumatol; 22 1825 1828
52 - Talkoff-Rubin NE, Cotran RS, Rubin RH. 2008Urinary tract infection, pyelonephritis, and reflux nephropathy. In: Brenner BM (editor). Brenner and Rector’s The Kidney. Saunders Elsevier, Philadelphia,;1203 1238
53 - Y. Tani, H. Tiwana, S. Hukuda, J. Nishioka, M. Fielder, C. Wilson, et al. 1997Antibodies to Klebsiella, Proteus and HLA-B27 peptides in Japanese patients with ankylosing spondylitis and rheumatoid arthritis. J Rheumatol;24 109 114
54 - C. Thomson, A. Armitage, 2010Urinary tract infection. In: Warrell DA, Cox TM, Firth JD (editors). Oxford Textbook of Medicine. Oxford University Press, Oxford,;4103 4122
55 - M. Tishler, D. Caspi, Y. Aimog, R. Segal, M. Yaron, 1992Increased incidence of urinary tract infection in patients with rheumatoid arthritis and secondary Sjogren’s syndrome. Ann Rheum Dis;51 604 606
56 - H. Tiwana, C. Wilson, P. Cunningham, A. Binder, A. Ebringer, 1996Antibodies to four gram-negative bacteria in rheumatoid arthritis which share sequences with the rheumatoid arthritis susceptibility motif. Br J Rheumatol;35 592 594
57 - H. Tiwana, C. Wilson, R. S. Walmsley, A. J. Wakefield, MS Cox. N. L. Smith, et al. 1997Antibody response to gut bacteria in ankylosing spondylitis, rheumatoid arthritis, Crohn’s disease and ulcerative colitis. Rheumatol Int;17 11 16
58 - J. P. Vandenbroucke, R. Kaaks, H. A. Valkenburg, J. W. Boersma, A. Cats, J. J. Festen, et al. 1987Frequency of infections among rheumatoid arthritis patients, before and after disease onset. Arthritis Rheum;30 810 813
59 - A. Wanchu, S. D. Deodhar, M. Sharma, V. Gupta, P. Bambery, A. Sud, 1997Elevated levels of anti-Proteus antibodies in patients with active rheumatoid arthritis. Ind J Med Res;105 39 42
60 - R. H. Weisbart, Y. Min, A. L. Wong, J. Kang, S. Kwunyeun, A. Lin, et al. 2005Selective IgA immune unresponsiveness to Proteus mirabilis fumarate reductase A-chain in rheumatoid arthritis. J Rheumatol;32 1208 1212
61 - C. Wilson, A. Ebringer, K. Ahmadi, J. Wrigglesworth, H. Tiwana, M. Fielder, et al. 1995Shared amino acid sequences between major histocompatibility complex class II glycoproteins, type XI collagen and Proteus mirabilis in rheumatoid arthritis. Ann Rheum Dis;54 216 220
62 - C. Wilson, D. Thakore, D. Isenberg, A. Ebringer, 1997Correlation between anti-Proteus antibodies and isolation rates of P. mirabilis in rheumatoid arthritis. Rheumatol Int;16 187 189
63 - C. Wilson, T. Rashid, H. Tiwana, H. Beyan, L. Hughes, S. Bansal, et al. 2003Cytotoxicity responses to peptide antigens in rheumatoid arthritis and ankylosing spondylitis. J Rheumatol;30 972 978
64 - W. Zhang, A. H. Anis, 2011The economic burden of rheumatoid arthritis: beyond health care costs. Clin Rheumatol;30 (Supp 1):S25 32